GMP Certification in Singapore

Certvalue is one of the Leading GMP Consultant  in Singapore for providing GMP Certification in Singapore, Hougang, Tampines, Pasir Ris, Yishun, Choa Chu Kang, Toa Payoh, Bukit Batok, Queenstown, Clementi, Serangoon, Sembawang and other major cities in Singapore with the services of implementation, Documentation, Audit, Templates, training, services, gap analysis, registration process at affordable cost to all organization to get certified under Good Manufacturing Practice management system in Singapore.GMP certification in Singapore everyone involved in the manufacturing processing of FDA regulated products as the responsibility to do the best to ensure that every product being manufactured is safe your and effective at the highest possible quality. Good manufacturing practices is a government regulation. The good manufacturing practice regulation establishes minimum standards for the manufacture of the product to prevent adulteration. But more importantly good manufacturing practices needs to be a Lifestyle where is company clearly defined implements through its quality management system in order to protect the health and safety of profits customers. Good manufacturing practice certification in Singapore  focuses more on the 10 principles of the standard which specifies on writing the step-by-step operating hand work instructions that provide the road map for GMP compliance on controlled and consistent performance. Carefully following and instructions to prevent decontamination mix ups and arrows. Promptly and accurately documenting your work for compliance and tractability. Ruin your systems do what they are designed by validating your work. Integrating the productivity, product quality and employee safety into the design and constructing facility and equipment.

GMP registration services in Singapore focuses on properly maintaining the facilities and equipment, clearly defining developing and demonstrating the job competence, protecting your products against the contamination by making cleanliness and hygiene a daily habit, building quality into into your product by systematically controlling your components and products related processes such as manufacturing, labeling, testing, distribution and marketing and controlling frequent audits on your management system. GMP in Singapore focuses on above mentioned that provides the perfect Framework for building and implementing mi Lifestyle and evaluating how you are living up to the standard of good manufacturing practices. GMP audit services in Singapore plays a vital role in helping the company to identify the hidden logos with in the system.

The consultant GMP certification in Singapore should be the right person to help you to implement the standard requirement in order to drive the system to achieve the intended output. As they have the expertise in implementing the standard across every industrial sector they should be the right person to help you to obtain the industrial best practices. The consultant of GMP Certification  in Hougang should make sure that their availability for implementing the standard he is assured which is one of the challenges faced by every companies during the implementation. GMP Certification in Singapore is the standard which is now being practiced across all the pharmaceutical companies as they have to mandatory get complied with the standard in order to export the products into European and US markets.

What are the advantages from the standard?

  • GMP consultancy services in Singapore helps your company brand value to be increased both in International and Domestic markets resulting in increased profit.
  • GNP consultancy in Singapore helps to identify all the risk involved in your process which might impact on the product quality.
  • GMP Consulting Services in Singapore is one of the industry specific standard which will help you to streamline the process efficiency.
  • Good manufacturing practice certification in Singapore helps you to eliminate the problem of customer satisfaction and customer complaints handling.

If we consider any of the manufacturing industries it will have certain rules and regulation and the procedures to carry out the whole process of the product when it is been manufactured, the first step will be collecting of raw materials, checking the quality of the raw materials, storing the raw materials, and next is the raw materials will be  supplied to the production, and when the processing will takes place like every organization will follow the same procedures, but in order to have the good practices one has to store the raw material without any damages and  use a good  raw materials that is of high quality and the production line with the necessary equipment should be provided to reduce the risks of accidents. In order to safeguard the employees, if there is any risk of accidents during the processing, mask and gloves have to be provided, suppose if they are working in chemical Industries it is mandatory to use the gloves and mask because those Chemicals are very harmful to the human body so the necessary and best practices has to be adopted in an industries to overcome these kind of problems and  finally when the product is ready the final testing has to be done to make sure that the product which are being manufactured is proper and it is  working properly and it is good quality so that when it is sold to the customers no complaints should be received so they always try to focus on the customer satisfaction and provide high quality products due to which if the products are good the customers will be more and hence the brand value also increases.

There are many documents that has to be considered while undergoing GMP certification in Tampines as it depend on the different companies process , now let us see what the required documents for medical field are:

  1. Application for an issuance of certificates on conformity according to GMP requirements i.e., the details in the language of an applicant that is understood by him.
  2. Registration copies of the drugs, and these documents should be submitted by having the stamp or signature of the applicant because it acts as a proof that be considered.
  3. Certified copy of documents which is official, and which has the right to carry out the activities for the production of medicine and other relevant state authority of the country where the production is located and the manufacturer has to provide lists of his official site which is authenticated by the signature or stamp of the applicant.
  4. Copies of the production site that is a site of the master file, because we should have clear glance that where it stated or where it got originated.
  5. The applicant copy or report which is certified and compiled from the latest inspection by the authority has to be considered. Where the inspection has to be made not more than 3 years which is prior to the application because these kinds of things has to be considered in order to make the process effective and acts a proof for future references.
  6. The documents related to the information on the last inspection that is carried out by the World Health Organization for training program and this inspection should not carry out more than 3 years which is prior to the application.
  7. For the quality of the product what are the references chosen should be filled in an application by his language because we will not be knowing he would have referred for the products quality and this will be helped by the GMP consultants in Singapore
  8. Based on inspections of manufacturing sites, conducted by the state control on which the references are taken should be mentioned by the applicant.
  9. And the list of medicines that are a registered or planning to be registered has to be specified in the application and the other copies which has to be submitted in the writing and in an electronic form are the copies of medical product certificates for an international trading.
  10. And the guarantee letter of their organization, that is completed in the language of an applicant.

In case of any medical industry or any pharmaceutical industries these are the documents required in order to complete  the GMP certification process in Singapore

How to get certified for GMP certification in Singapore?

Global consulting companies for consultation and certification for all the international standards which are available in market with Consulting experience across 20 different management standards having capabilities to deliver the management system benefits across 30 different countries which makes us better compared to others. We have hundred percent track record of success in successful implementation of management system and Audit clearance. With us the cost of GMP certification in Singapore is always feasible for all of our customers which is one of the extra added value.

How to get GMP Consultant in Singapore?

If you are looking how to get GMP certification in Singapore you are at the right place as we are one of the one stop solution provider for your certification requirement. You have to just write to us at [email protected] or visit our official website at no more about this. Help desk person and will be available 24/7 in order to register your certification requirement and we assure for our consultants call back at the earliest in order to understand your requirement better and help you to get certified at affordable cost.

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Conduct Gap Analysis to find any Shortcomings from the standard requirements.


Policies, procedures, Work Instructions, Evidences, Records, Training


Conduct frequent internal audit and management review meeting.


Apply corrective actions on the identified root cause or shortcomings






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Enhancement of Performance

ISO certification is a tool to streamline and enhance the process performed internal to the organization. Certvalue indulges in inculcating best industry practices.


Recognition and Brand Value

It is always about the Brand value of your organization in the market and ISO certification from Certvalue can make your organization to be an excel and stand out in the market globally


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ISO certification is a basic requirement to bid or participate in any tenders floated by government or private sector. And ISO certification from Certvalue is an assurance win over the tenders.

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