Ecovadis Overview 

Global Corporate Sustainability Assessment 

Ecovadis is the world’s leading platform for corporate sustainability assessment, helping organizations around the globe measure, manage and improve sustainability performance. In the context of society’s increasing interest in social responsibility, environment and governance (ESG), Ecovadis has become an indispensable partner, helping businesses meet the requirements of the market, customers and stakeholders for sustainable development. 

About Ecovadis 

Ecovadis was founded in 2007 in France, with the goal of building an objective and transparent assessment platform for the sustainability of businesses and supply chains. Through the development process, Ecovadis has evaluated tens of thousands of companies in more than 200 industries and more than 160 countries around the world. 

The Ecovadis platform works based on collecting data from businesses, analyzing according to international criteria, and providing assessment results through scores and rankings. This result helps organizations identify strengths and weaknesses and develop improvement plans that are aligned with business practices. 

Why is Ecovadis important? 

  • Customers, partners, and supply chains: More and more global corporations require suppliers to achieve a certain Ecovadis score in order to maintain cooperation. This helps ensure that products and services are provided from a responsible and transparent value chain. 
  • Risk management: Ecovadis’ assessment helps businesses identify potential risks related to the environment, human rights, business ethics and governance. 
  • Improve brand reputation: Businesses with high scores in the Ecovadis system are often identified by multinational companies and large customers as a reliable partner, increasing opportunities for international cooperation. 
  • Promoting continuous improvement: Based on the assessment report, businesses develop specific action programs to improve sustainability and social responsibility. 

Ecovadis evaluation criteria 

Ecovadis uses an assessment framework based on four central themes: 

  • Environment: Including optimal management of resources, reduction of greenhouse gas emissions, waste management, use of renewable energy, compliance with international environmental standards and internal policies of the enterprise. 
  • Human rights and labor: Assessing labor rights, health and safety, diversity and inclusion, discrimination prevention, protection of children’s rights, and policies on human resource training and development. 
  • Business ethics: Consider policies to prevent corruption, bribery, financial transparency, information security, respect for intellectual property rights, and comply with the law. 
  • Supply chain management: Evaluate transparency, responsibility in partner selection, supply chain risk management, and the impact of supply chain on the above topics. 

Ecovadis Assessment Process 

Ecovadis’ assessment process includes the following steps: 

  • Registration and provision of information: Businesses register on the Ecovadis platform, provide relevant documents and data. 
  • Data analysis: Ecovadis uses a team of experts and data analysis technology to evaluate the company’s records, documents, policies, certificates, and management processes based on international standards (ISO, GRI, UNGC, etc.). 
  • Scoring and ranking: Ecovadis evaluates key topics, scores each area, and aggregates them into an overall score (usually from 0 to 100). 
  • Reports and feedback: Businesses receive detailed transcripts and reports, providing a roadmap for improvement and specific recommendations. 
  • Periodic re-evaluation: Businesses can update data, demonstrate improvements, and request a re-evaluation after a certain period of time (usually annually). 

Meaning of Ecovadis Score 

The results of the Ecovadis assessment are shown through ratings, from Bronze, Silver, Gold to Platinum, based on the average score of the business compared to the industry and region: 

  • Copper: Meet the minimum requirements for sustainable development. 
  • Silver: There are effective policies and actions on sustainability. 
  • Gold: Rated as a leader in responsibility and continuous improvement. 
  • Platinum: Excellent achievements, meeting the highest standards of corporate sustainable development. 

Achieving these levels not only supports businesses in international cooperation but also helps increase the trust of investors, customers and the community. 

Benefits of participating in Ecovadis 

  • Optimize business governance: Ecovadis helps identify gaps in the management system, thereby improving operational efficiency and compliance. 
  • Access to new markets: Many corporations and partners only work with businesses with Ecovadis ratings, opening up opportunities to cooperate with large global customers. 
  • Promote continuous improvement: The Ecovadis Scorecard is the basis for businesses to build a sustainable improvement action program according to a clear roadmap. 
  • Improve reputation and image: Achieving Ecovadis certification helps businesses affirm their position, attract investment and recruit talents. 

Challenges and development trends 

Although Ecovadis offers many benefits, the assessment process also poses many challenges: 

  • Businesses need to invest in management systems, standardize processes and make data transparent. 
  • It requires coordination between many departments in the organization: human resources, environment, legal, finance, supply chain, etc. 
  • Continuously update new regulations on sustainable development on a global scale. 

The current trend is that more and more businesses in Vietnam and the world are actively participating in Ecovadis, turning sustainability criteria into competitive drivers, promoting innovation and international integration. 

Ecovadis has become an important tool to help businesses promote sustainable development, improve their reputation and expand global business opportunities. Participating in this assessment system is not only a requirement from customers and partners but also a commitment of businesses to society, the environment and future generations. Ecovadis is constantly improving and updating standards to catch up with development trends, supporting businesses to affirm their pioneering role in the green and comprehensive sustainable transformation. 

CONTACT FOR SERVICE SUPPORT:

Contact Vietnam representative: Duc Luong Services

Hotline: +84 933096426 – +84 868 591 260

Email: info.vietnam@iscglobal.asia – van.pham@iscglobal.asia – ducluongservices@gmail.com

REGISTER FOR SERVICE HERE: APPLICATION FORM!

TGA Training, Consulting and Certification Services – Therapeutic Goods Administration (Australia) 

The gateway to the Australian pharmaceutical and medical device market 

About TGA – Therapeutic Goods Administration 

The Therapeutic Goods Administration (TGA) is the regulatory body of the Australian Government responsible for evaluating, supervising and approving pharmaceutical products, medical devices and other healthcare products before they are allowed to circulate on the Australian market. TGA ensures that all of these products meet stringent safety, efficacy, and quality standards to protect public health. 

In addition to acting as a regulatory body, TGA also provides training, consulting and certification services to support businesses, organizations and individuals in the process of developing, registering and operating products in the Australian market. 

TGA Training Services 

TGA organizes a variety of training programs, from basic to advanced, for subjects such as manufacturers, distributors, medical experts, researchers and organizations related to the field of pharmaceuticals and medical devices. These trainings are typically designed to: 

  • Provide in-depth knowledge of the current legal regulations related to medicines, medical devices, supplements, biologicals, in vitro diagnostics and cosmetic products in Australia. 
  • Guiding the process of filing, evaluating and approving products according to TGA standards. 
  • Raise awareness of product safety, risk management, and after-sales monitoring processes. 
  • Training on quality management systems, GxP STANDARDS (GMP, GDP, GCP, GLP) and related international standards. 
  • Stay up to date with the latest changes in TGA’s health management regulations and policies. 

The courses often combine theory and practice, using real-life situations, group exercises, and simulations of the product registration process to give students a comprehensive, practical view. In particular, TGA also organizes online seminars, training programs according to the specific requirements of businesses as well as in-depth courses for each specific product field group. 

TGA Consulting Services 

TGA and its authorized partners provide comprehensive consulting services to businesses and organizations wishing to bring their products to the Australian market or ensure compliance with TGA regulations. The contents of the consultation include: 

  • Analyze and evaluate the legality and appropriate roadmap for products to meet TGA standards. 
  • Assisting in developing product registration strategies, preparing dossiers, scientific evidence, technical documents, and supporting communication with regulators. 
  • Evaluate the internal quality management system, support improvement to meet GMP (Good Manufacturing Practice) standards or other relevant certifications. 
  • Advising on issues related to product changes, risk management, safety warnings, product recalls, and medical incident reporting. 
  • Guide enterprises to solve problems in the process of post-inspection, periodic inspection or when inspected by TGA. 
  • Train and build the capacity of personnel to meet quality control requirements and comply with legal regulations. 

In addition, the consultant also supports businesses in market research, identifies opportunities and challenges, optimizes product commercialization roadmaps in Australia, thereby minimizing risks and development costs. 

TGA Certification Services 

In order for a pharmaceutical product, medical device or other healthcare product to be allowed to circulate on the Australian market, the product owner must comply with the TGA’s strict certification process. TGA’s certification services include: 

  • Legality checks, document checks, and comprehensive evaluations of product safety, efficacy, and quality. 
  • Carry out tests, technical verifications, production process inspections, and clinical trials (if necessary). 
  • Evaluate and inspect the quality management system of the enterprise according to GMP standards or appropriate ISO standards. 
  • Appraisal and issuance of ARTG (Australian Register of Therapeutic Goods) codes for standard products, allowing them to be legally circulated in Australia. 
  • After-sales supervision, periodic inspection, and handling of problems arising during product circulation on the market. 

The TGA certification process often consists of many complex steps, requiring close coordination between businesses, consulting organizations and regulatory agencies. Obtaining certification from the TGA not only helps the product reach the Australian market but also improves its reputation and expands export opportunities to other international markets. 

Benefits of TGA training, consulting and certification services 

Participating in and successfully meeting the TGA training, consulting and certification processes brings many practical benefits to businesses and organizations: 

  • Improve knowledge and capacity to comply with the law in the Australian market. 
  • Quickly and effectively access the large and potential pharmaceutical and medical device markets. 
  • Minimize legal, financial and reputational risks during product commercialization. 
  • Improve brand value, reputation and trust of partners and consumers in Australia and internationally. 
  • Increase the ability to transfer technology and international cooperation by meeting the high standards of the TGA. 
  • Optimize the product development process, save time and costs thanks to a clear roadmap. 

Product registration and certification process with TGA 

To register and certify products according to TGA regulations, businesses need to take the following basic steps: 

  • Assess the conformity and determine the type of product according to the classification of the TGA (drugs, medical devices, biologicals, cosmetics, etc.) 
  • Prepare and complete a set of technical documents, scientific documents, evidence of product safety and effectiveness. 
  • Submit the registration dossier to the TGA’s online system, and pay the appraisal fee as prescribed. 
  • Wait for reviews, feedback, and additional information if requested. 
  • Once approved, receive the ARTG number and the product circulation license in Australia. 
  • Perform after-sales supervision obligations, report incidents (if any) and comply with periodic inspection regulations. 

Products in high-risk groups (e.g., implantable medical devices, new drugs, complex biologics) often require preclinical studies, clinical trials, or more in-depth evaluations before being approved for marketing. 

The TGA plays a key role in ensuring the safety, quality and effectiveness of healthcare products in Australia. Through training, consulting and certification services, TGA not only supports businesses to access the Australian market but also contributes to improving operational standards, promoting the sustainable development of the pharmaceutical – medical device industry in particular and the healthcare sector in general. 

Understanding and complying with TGA regulations, as well as effectively utilizing related support services, will be the key for businesses and organizations to achieve success, expand their scope of operations and affirm their position in today’s competitive international market.

CONTACT FOR SERVICE SUPPORT:

Contact Vietnam representative: Duc Luong Services

Hotline: +84 933096426 – +84 868 591 260

Email: info.vietnam@iscglobal.asia – van.pham@iscglobal.asia – ducluongservices@gmail.com

REGISTER FOR SERVICE HERE: APPLICATION FORM!

Overview of TGA Certification – Therapeutic Goods Administration (Australia) 

Discover the role, process and significance of the TGA in the Australian health sector 

About the Therapeutic Goods Administration (TGA) 

The Therapeutic Goods Administration (TGA) is Australia’s national health regulator, under the Department of Health. The TGA is responsible for administering, evaluating, licensing and monitoring all therapeutic goods used in Australia – including medicines, vaccines, medical devices, diagnostic instruments, therapeutic cosmetics, supplements and blood or blood products. 

The TGA plays a central role in protecting public health by ensuring that medical products circulating in Australia meet safety, quality and efficacy standards. Any business that wants to bring a therapeutic product into the Australian market must comply with the regulations and go through a rigorous review process by the TGA. 

Role and scope of management of the TGA 

  • Evaluation and licensing of new therapeutic goods to the Australian market. 
  • Post-market monitoring to ensure products continue to meet safety standards. 
  • Updates, adjustments, or recalls of unsafe products. 
  • Formulate and maintain standards and technical regulations for therapeutic goods. 
  • International cooperation, sharing information and experience with global health regulators. 

Classification of therapeutic goods by TGA 

The TGA regulates a wide range of therapeutic goods, including: 

  • Medicines: prescription drugs, over-the-counter drugs, complementary medicines, vaccines, blood products, herbal medicines. 
  • Medical Devices: machines, instruments, diagnostic test tubes, assistive devices, and implants. 
  • Complementary Medicines: vitamins, minerals, herbs, dietary supplements. 
  • Biologicals: stem cells, biological tissues, biological vaccines. 

The products are classified based on the level of risk. High-risk products will be subject to stricter controls. 

TGA Registration and Certification Process 

1. Determine the type of product and classify the risk 

Businesses need to accurately determine the type of therapeutic goods and the risk level of the product. The correct classification is an important step, deciding the next review process. 

2. Prepare the registration dossier 

Records include technical literature, clinical or non-clinical data, information on ingredients, manufacturing processes, quality standards, labels, instructions for use, and evidence of efficacy and safety. 

3. Submit dossiers and scientific assessments 

The TGA will review the records, evaluate the data, and may request additional information or conduct additional tests. For new or complex products, the review process can take 6-18 months or more depending on the case. 

4. Register with ARTG (Australian Register of Therapeutic Goods) 

If the product fully meets the requirements for safety, quality, and efficacy, it will be registered in the Australian Therapeutic Goods Register (ARTG). Only products named in the ARTG are allowed to be imported, manufactured, distributed and sold in Australia. 

5. Supervision and post-inspection 

After licensing, the TGA continues to monitor the product through a problem reporting system, periodic inspections, and product recalls if new risks are detected. 

Meaning of TGA Certification 

TGA certification is a mark that confirms that a therapeutic product has passed Australia’s stringent safety and efficacy standards. This offers many benefits: 

  • Increased credibility and reliability: TGA certified products are recognized in many other developed countries. 
  • Expand access to global markets: Many international markets refer to the TGA standard when considering licensing. 
  • Public health protection: Thanks to strict control, potential risks are detected and eliminated in a timely manner. 
  • Support businesses: Transparent and clear processes help businesses build effective product development strategies. 

Challenges of obtaining TGA certification 

  • The evaluation process is long and complicated: Requires thorough dossier preparation and complete scientific data. 
  • High cost: Includes the cost of testing, evaluation, clinical trials, and registration fees. 
  • Requirements for compliance with international quality standards: Production and inspection must comply with international standards (GMP, ISO, etc.) 
  • Regularly update and change regulations: Businesses need to keep a close eye on changes in Australian law. 

Compare TGA Certification with other international certifications 

  • TGA and FDA (US): Both agencies have rigorous review processes, but standards and documentation requirements may differ. Some products that have been approved by the FDA still need to be resubmitted according to TGA standards when entering Australia. 
  • TGA and CE Marking (Europe): CE focuses on product safety and performance when circulating in the European market; The TGA has tighter control over testing and after-sales supervision. 
  • Mutual recognition: Australia participates in a number of international agreements that ease the formalities with products that have been approved in a number of other developed markets. 

Notes when preparing for TGA certification 

  • Understand the type of product and applicable regulations. 
  • Prepare scientific documentation, complete and transparent testing. 
  • Contact experienced experts or consultants about the Australian market. 
  • Ensure the production process and quality management meet international GMP and ISO standards. 
  • Regularly monitor the TGA website for the latest regulations. 

TGA certification is a mandatory “passport” for therapeutic products wishing to enter the potential Australian market and is also a testament to the quality of products at the international level. Meeting the TGA requirements not only protects the health of users but also helps businesses improve their reputation, expand export markets and develop sustainably in the global health sector.

CONTACT FOR SERVICE SUPPORT:

Contact Vietnam representative: Duc Luong Services

Hotline: +84 933096426 – +84 868 591 260

Email: info.vietnam@iscglobal.asia – van.pham@iscglobal.asia – ducluongservices@gmail.com

REGISTER FOR SERVICE HERE: APPLICATION FORM!

GRS (Global Recycled Standard) Supplier Assessment Service

Solutions to ensure sustainable and environmentally responsible supply chains 

About GRS – Global Recycled Standard 

GRS (Global Recycled Standard) is an international standard developed by Textile Exchange that confirms the recycled content of products, while ensuring social, environmental and chemical responsibility requirements in the production process. GRS is widely applied in the textile, footwear, packaging, plastics and related industries of recycled materials. 

Importance of GRS Provider Assessment 

Supplier audits according to GRS standards help businesses: 

  • Ensure transparency and traceability of recycled materials. 
  • Affirming its commitment to sustainable development and environmental protection. 
  • Expand export markets to countries that require strict environmental standards. 
  • Create competitive advantages, improve brand reputation with partners and consumers. 

GRS Supplier Assessment Service Content 

GRS provider assessment services typically include: 

  1. Documentation and process review: Check documents and records related to the origin, percentage of recycled materials, and production processes. 
  1. Site inspection: The audit team will conduct a field survey at the factory to confirm compliance with GRS regulations on material management, chemicals, environment and social responsibility. 
  1. Training and consulting: Supporting suppliers to understand requirements, building a management system in accordance with GRS standards. 
  1. Reports and recommendations: Provide detailed reports on compliance, suggesting areas for remediation (if any). 
  1. Certification: After fully meeting the requirements, the supplier will be granted an internationally valid GRS certification. 

Benefits of taking a GRS assessment 

  • Increase customer confidence: Products with GRS certification are highly appreciated by domestic and foreign markets. 
  • Responding to green consumption trends: Consumers are increasingly interested in products that are environmentally friendly and have clear origins. 
  • Minimize legal risks: Comply with environmental, labor, and chemical regulations. 
  • Expand partnerships: Easily cooperate with big brands, international retail chains that require sustainability standards. 

GRS Supplier Evaluation Process 

  1. Receive registration and preliminary survey of business needs. 
  1. Support businesses to prepare documents and train awareness about GRS. 
  1. Conduct an on-site audit. 
  1. Report the results and instructions for remediation (if there are inappropriate points). 
  1. It is proposed to issue GRS certification when the enterprise meets all the requirements. 

GRS supplier assessment service is the key to helping businesses affirm their position in the international market, demonstrating social and environmental responsibility. “One tree should not be young, three trees together make a high mountain” – together to build a sustainable supply chain, for a green future for future generations.

CONTACT FOR SERVICE SUPPORT:

Contact Vietnam representative: Duc Luong Services

Hotline: +84 933096426 – +84 868 591 260

Email: info.vietnam@iscglobal.asia – van.pham@iscglobal.asia – ducluongservices@gmail.com

REGISTER FOR SERVICE HERE: APPLICATION FORM!

GMP Standard Training Service 

Solutions to improve production and management quality in the pharmaceutical, food and cosmetics industry 

Introduction 

In the context of global economic integration and development, compliance with international standards for production is becoming increasingly important, especially in industries related to public health such as pharmaceuticals, food, and cosmetics. GMP (Good Manufacturing Practices) standards are a set of strict international standards to ensure that products are manufactured and controlled consistently and of the highest quality. 

Benefits of GMP Training 

  • Improve the awareness, skills and professional attitude of officers and employees in the enterprise. 
  • Minimize product quality risks, minimize errors in the production process. 
  • Increase brand reputation, create trust for partners and customers. 
  • Optimize production processes, save costs, and improve business efficiency. 
  • Meet the requirements of inspection and assessment of state management agencies and export markets. 

Forms of Training 

  • Direct training at the enterprise: Specialized program, suitable for each unit, combining theory and practical practice. 
  • Class-intensive training: Periodic courses at the training center with standardized syllabus and updating the latest knowledge. 
  • Online training: Flexible in time and place, suitable for personnel who are remote or have busy work schedules. 

GMP standard training content 

  1. Overview of GMP and related legal regulations. 
  1. Fundamentals and quality management processes. 
  1. Hygiene control of factories, equipment and production environment. 
  1. Manage records, documents, and product traceability. 
  1. Control of raw materials, semi-finished products, finished products. 
  1. Practical training in troubleshooting, risk assessment, and continuous improvement. 

Teaching Team 

The lecturers are leading experts in the field of GMP, rich in practical experience, having worked and consulted for many domestic and international businesses. The flexible teaching method, combining theory and practical sharing, makes it easy for students to absorb and apply effectively to their daily work. 

Quality Commitment 

GMP standard training services are committed to bringing practical value, closely following the actual needs of businesses. After the course, students will master the knowledge and skills necessary to operate, supervise and maintain a quality management system according to GMP standards, contributing to improving the position of businesses in the market. 

Contact for consultation & registration 

For more details about GMP training programs, please contact us for specific advice and to build a training path suitable for your business. “There is merit in sharpening iron, there is a day to make a needle” – Investment in training is an investment in the sustainable development of the business. 

CONTACT FOR SERVICE SUPPORT:

Contact Vietnam representative: Duc Luong Services

Hotline: +84 933096426 – +84 868 591 260

Email: info.vietnam@iscglobal.asia – van.pham@iscglobal.asia – ducluongservices@gmail.com

REGISTER FOR SERVICE HERE: APPLICATION FORM!

GMP Standard Consulting Service 

Solutions to ensure quality and improve reputation for manufacturing enterprises 

General Introduction to GMP 

GMP (Good Manufacturing Practices) is a set of mandatory international standards in the field of food, pharmaceuticals, cosmetics and medical device manufacturing. GMP compliance not only helps businesses ensure product quality and safety for consumers, but also creates a competitive advantage in the domestic and international markets. 

Benefits of applying GMP 

  • Effectively control the production process, minimize quality risks. 
  • Increase the trust of customers and partners, expand export opportunities. 
  • Comply with the provisions of the law and strict requirements from regulatory agencies. 
  • Minimize waste and save costs by optimizing the production process. 
  • Improve the image, reputation and brand value of the enterprise. 

Content of GMP consulting services 

Our GMP consulting services provide a comprehensive solution, accompanying businesses from assessing the current status to building, applying and maintaining a standard GMP system.

  1. Survey & Assessment of the Current Status: Evaluate the current management system, facilities, personnel and production process of the enterprise. 
  1. Develop a GMP implementation plan: Provide a detailed roadmap in accordance with the actual conditions of the business. 
  1. Training & awareness raising: Organize training courses for managers and employees on GMP standards and good practices. 
  1. Support to improve facilities: Consulting on the design, layout of factories, equipment systems in accordance with GMP requirements. 
  1. Develop system documentation: Draft processes, work instructions, and record forms according to GMP standards. 
  1. Adoption & Monitoring Support: Accompanying the implementation process, internal audit and preparation for certification audit. 
  1. GMP certification consulting: Assisting businesses in working with certification bodies, completing documents and meeting audit requirements. 

Why choose our consulting services? 

  • A team of experts with many years of experience in the field of GMP, having successfully consulted hundreds of businesses. 
  • Flexible solution, cost optimization, suitable for each type of production. 
  • Committed to accompanying and supporting businesses until they achieve GMP certification. 
  • Dedicated after-sales service, ready to support businesses in the process of maintaining the GMP system in the future. 

Service Registration Process 

  1. Receive information and free preliminary consultation by phone or email. 
  1. Actual survey and appropriate service quotation. 
  1. Signing the contract and implementing the detailed consulting plan. 
  1. Supporting businesses to achieve certification and maintain the system for a long time. 

Contact us 

Don’t let your business “water to the feet before jumping”. Let’s proactively build a quality management system according to GMP standards today to “eat strong and durable”, affirm our position in the market. 

Contact us now for a free consultation and get the best quote!

CONTACT FOR SERVICE SUPPORT:

Contact Vietnam representative: Duc Luong Services

Hotline: +84 933096426 – +84 868 591 260

Email: info.vietnam@iscglobal.asia – van.pham@iscglobal.asia – ducluongservices@gmail.com

REGISTER FOR SERVICE HERE: APPLICATION FORM!

GMP Certification Services 

Solutions to improve product quality and reputation 

About GMP Certification 

GMP (Good Manufacturing Practice) is a system of standards and processes to ensure that products are manufactured consistently in terms of quality, safety, and suitability for their intended use. GMP certification is a testament to your commitment to complying with strict hygiene regulations, controlling the manufacturing process, preservation and distribution of products. 

Benefits of GMP certification 

  • Improve reputation: Businesses are highly appreciated by customers, partners and management agencies for product quality. 
  • Meet legal regulations: Many industries such as food, pharmaceuticals, cosmetics… GMP certification is required for product circulation. 
  • Market expansion: GMP certification is a “passport” for products to enter fastidious domestic and foreign markets. 
  • Risk Control: Minimize the risk of product recalls, claims, or harm to consumers. 
  • Process optimization: Applying GMP helps businesses save costs and improve production efficiency. 

Content of GMP Certification Services 

GMP certification services typically include the following steps: 

  1. Survey and assess the current status of factories and production facilities. 
  1. Consulting on building and completing the system of documents and processes according to GMP standards. 
  1. Train personnel on GMP knowledge, operation and supervision skills. 
  1. Support the improvement of production and preservation facilities, equipment. 
  1. Support businesses to register, prepare documents and work with certification organizations appointed or recognized by the Ministry of Health. 
  1. Periodic evaluation and supervision to maintain and improve the efficiency of the GMP system. 

Industries applying GMP 

GMP certification is widely applied in many fields such as: 

  • Foods and dietary supplements 
  • Pharmaceutical product 
  • Cosmetic 
  • Medical Devices 
  • Animal feed and aquatic products 

It can be said that “the kitchen must be clean, the market must be fresh” is a testament to the spirit of “prevention is better than cure” of the Vietnamese people. GMP certification services not only help businesses improve product quality but also contribute to building solid trust with customers and partners. Investing in GMP is an investment in the sustainable and long-term development of businesses in the era of international integration.

CONTACT FOR SERVICE SUPPORT:

Contact Vietnam representative: Duc Luong Services

Hotline: +84 933096426 – +84 868 591 260

Email: info.vietnam@iscglobal.asia – van.pham@iscglobal.asia – ducluongservices@gmail.com

REGISTER FOR SERVICE HERE: APPLICATION FORM!

CQI Standards Training & Consulting Services 

Solutions to improve the quality of business management and operation 

About CQI Training & Consulting Services 

CQI (Continuous Quality Improvement) standard training and consulting service is a strategic solution for businesses that want to improve management efficiency, improve operational processes and increase competitiveness in the market. With the motto “There is merit in sharpening iron, there is a day to make a needle”, CQI helps the organization gradually improve the quality management system, in accordance with operational practices and long-term development goals. 

Benefits of implementing CQI 

  • Improve work efficiency: CQI helps optimize processes, minimize errors and waste, and increase labor productivity. 
  • Improve the quality of products/services: Continuously evaluate and improve, ensuring that products/services always meet the highest standards. 
  • Create a learning and development environment: Encourage employees to actively propose ideas for improvement, build a positive corporate culture. 
  • Increase customer satisfaction: Stable and improved quality helps businesses maintain customer trust. 
  • Compliance with international regulations and standards: CQI makes it easy for businesses to meet ISO, HACCP, GMP, and related legal requirements. 

CQI Training & Consulting Content 

  1. Introduction to CQI and its foundational principles. 
  1. Analyze the current status of the process, identify points for improvement. 
  1. Develop a quality improvement plan based on actual data. 
  1. Implement quality control tools such as PDCA, Six Sigma, Lean. 
  1. Train personnel on innovative thinking and CQI practice skills. 
  1. Evaluate results, maintain and improve improvement efficiency. 

CQI Service Deployment Process 

Step Describe 
1 Survey and assessment of the current state of the enterprise 
2 Develop appropriate training and consulting programs 
3 Conduct on-site or online training and instruction 
4 Monitoring and supporting the implementation of improvements 
5 Evaluate results, adjust and sustain improvements 

Why choose CQI Training & Consulting Services? 

With the companionship of experienced experts, businesses will have access to modern quality improvement methods, suitable for industry characteristics. “Go one day, learn a wise one” – through CQI training and consulting, the organization not only improves internally but is also ready to reach far in the international market. 

If you are interested in CQI standard training and consulting services, please contact us for detailed advice and build the most suitable solution for actual needs.

CONTACT FOR SERVICE SUPPORT:

Contact Vietnam representative: Duc Luong Services

Hotline: +84 933096426 – +84 868 591 260

Email: info.vietnam@iscglobal.asia – van.pham@iscglobal.asia – ducluongservices@gmail.com

REGISTER FOR SERVICE HERE: APPLICATION FORM!

CQI Standard: Overview

Understanding Continuous Quality Improvement in Quality Management

About CQI

CQI (Continuous Quality Improvement) is a management method that focuses on continuously improving processes, products, or services in an organization. Instead of just solving problems as they arise, CQI aims to proactively seek opportunities for improvement, ensuring quality is enhanced every day. The idiom “There is merit in sharpening iron, there is a day to make a needle” is very suitable to describe the spirit of perseverance of CQI in improving every small step.

Fundamentals of CQI

Continuous: Improvement is not a one-time process, but an iterative process.

Data-driven: Improvement decisions are based on the analysis of actual metrics.

Team: Encourage the participation of all members of the organization.

Customer-centric: Every improvement is geared towards enhancing customer satisfaction.

CQI Implementation Process

The CQI process typically includes the following steps:

  • Identify the problem: Identify the areas that have not been met or need improvement in the process.
  • Data collection and analysis: Use metrics to identify the root cause of problems.
  • Improvement planning: Develop an improvement plan based on analysis.
  • Implement improvements: Implement the proposed solutions.
  • Evaluate the results: Check that the solutions are working as expected.
  • Maintain and expand: Apply successful improvements to a wider scope.

Benefits of CQI

Improve the quality of products/services in the long term.

Minimize errors, waste, and operating costs.

Engage employees, create a positive working environment.

Increase customer and partner satisfaction.

Application of CQI in practice

CQI is widely applied in many sectors such as manufacturing, healthcare, education, and services. For example, in the healthcare industry, CQI helps improve the quality of patient care by improving the medical examination and treatment process. The proverb “Knowing the person who knows me, a hundred battles and a hundred wins” shows the need to understand the process and the current situation to improve efficiency.

The CQI standard is not only a set of rules, but also a modern management philosophy that helps the organization develop sustainably. Applying CQI is a long-term investment, bringing value to businesses, employees and customers. When “one tree should not be young, three trees together make a high mountain”, collective consensus is the key to success with CQI.

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GPSR Standards Overview 

General Product Safety Requirements

About GPSR Standards

GPSR stands for “General Product Safety Requirements”. It is a set of legal standards or regulations intended to ensure that products placed on the market must meet the minimum requirements for consumer safety, avoiding endangering health or life under normal or reasonable conditions of foreseeable use.

Purpose and Meaning

The GPSR standard is designed to protect the rights and safety of consumers, and to enhance the responsibility of manufacturers, importers, and distributors for the products they provide to the market. GPSR compliance minimizes the risk of accidents, injuries, or negative health effects caused by unsafe use of the product.

The Basics of GPSR

  • General Safety Requirements: The product must be safe to use under normal or reasonably foreseeable conditions.
  • Responsibilities of stakeholders: Manufacturers, importers, distributors must ensure that products meet safety standards, inspect, monitor quality, and report potential risks if detected.
  • Assessment and inspection: Regularly inspect and evaluate products to detect potential risks early, recall products that do not meet safety requirements.
  • Information and labels: Products must have clear instructions for use, risk warnings (if any) and adequate labels, helping consumers to recognize and use them properly.

Scope of application

GPSR generally applies to most types of consumer products, except for some special cases that have separate safety regulations (such as pharmaceuticals, food, medical devices,…). In Europe, the GPSR standard is specified in Directive 2001/95/EC on general product safety, which is an important legal basis for controlling the quality of consumer goods on the market.

Impact on Businesses and Consumers

  • For businesses: GPSR compliance helps businesses build reputation, avoid legal risks, minimize the cost of recalling defective products and expand export markets.
  • For consumers: GPSR brings peace of mind when using products, contributing to improving the quality of life and protecting the interests of shoppers.

GPSR standards play a key role in ensuring product safety in the market, protecting public health and consumer rights. Businesses need to actively learn, update and comply with the requirements of GPSR for sustainable development and international integration. As the saying goes: “Prevention is better than cure”, ensuring product safety from the beginning will help businesses avoid many consequences later.

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Contact Vietnam representative: Duc Luong Services

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