GLP Certification in Cape Verde

Certvalue is the Leading GLP Consultant in Cape Verde for providing GLP Certification in Cape Verde, Praia, Santa Maria, Tarrafal, , Mindelo and other major cities in Cape Verde with the services of implementation, Documentation, Audit, Templates, training, gap analysis and registration process at affordable cost to all organization to get certified under good manufacturing management system in Cape Verde. GLP Certification in Cape Verde (Good Laboratory Practice) is a well-known acronym for quality in the laboratory GLP is a formal regulation that was formulated in 1978 by the US Food and Drug Administration (FDA) that registered the pharmaceutical manufactory but, the primary target of the regulation was not the chromatography laboratory nor even the analytical laboratory. GLP in Cape Verde was designed to regulate non-clinical laboratory safety (in animal toxicology testing) to assure that part of new molecular entities by the pharmaceutical manufactory were safe before administration to human volunteers and patients in clinical trials. Good Laboratory Practice Certification in Cape Verde has not changed since the regulation was published as the title of the regulation makes clear: Good Laboratory Practice for nonclinical Laboratory. While you may determine that the Laboratory in GLP in Cape Verde includes chromatography, the Fundamental aim of the regulation does not. The main laboratories that were affected by the regulation were one’s act histology, clinical chemistry, and pathology, which are used to evaluate the samples achieved from toxicology studies. In addition to the FDA regulations, the for Economic Cooperation and Development (OECD) has issued GLP regulations that we use in Europe that have the same overall intent as the FDA regulations but with some differences.

Principles of GLP Certification in Cape Verde?

The purpose of these Principles of GLP in Cape Verde is to boost the development of quality test data. Related quality of test data forms the basis for the mutual acceptance of data among countries. If respective countries can positively rely on test data developed in other countries, duplicate testing can be avoided, saving time and resources. The application of GLP Cost in Cape Verde should help to abstain from the creation of technical barriers to trade, and increase the protection of human health and the environment.
  1. Test Facility Management’s Responsibilities
  2. Quality Assurance Programme
  3. Facilities
  4. Apparatus, Material, and Reagents
  5. Test Systems
  6. Test and Reference Items
  7. Standard Operating Procedures
  8. Performance of the Study
  9. Reporting of Study Results
  10. Storage and Retention of Records and Materials.
Many organizations of varying types of Testing & calibration Companies, Medical Laboratory Companies are using GLP Certification Services in Ribeira Grande as a most recognized method of delivering customer pride and controlling quality of product and Service within their chosen sector. GLP not only can be used to supply enhancements and help assure quality, however the accreditation is often viewed as an assurance of uniformity of product and offerings throughout borders, languages, and cultural boundaries. Therefore, having GLP accreditation can be considered as fine on a reputation basis, as well as a practical one. Implementation of GLP Certification in Cape Verde is different from assurance of business. So that the Implementation can be done by GLP Consultants for all the industries in Cape Verde, GLP Services in Cape Verde improves the customer satisfaction by identifying their needs and goals. What is the importance of GLP Consulting Services in Cape Verde? GLP Certification registration in Cape Verde isn’t limited to chemicals only. GLP Certification Services in Cape Verde also addresses food additives, medical devices, color additives, food packaging, and other non-pharmaceutical products or ingredients. One of the main goals of GLP Consulting Services in Cape Verde is to control what scientists do and how they carry out their safety/quality testing of chemical and biochemical products as well as in development pharmaceuticals. GLP Certification in Cape Verde is also required for registration purpose and licensing of pharmaceuticals, food additives, veterinary drug products, pesticides, and some bio-products. GLP Certification Consultant in Cape Verde is aimed at proving that no safety and quality data has been manipulated or changed in one way or another. GLP Certification in Cape Verde also assures regulators and research Commands that the statistics and information which are being acknowledged are based on the study results and findings. Only this way can they progress and make the required assessments completely. GLP in Cape Verde minimizes fraudulent claims or any other discrepancies, analyses are required to keep sufficient, reliable, valid, consistent and correct records of every individual testing process, approach, and methodology.

How to get GLP Consultants in Cape Verde?

Certvalue is a leading Top GLP Consultants in Cape Verde for providing GLP Certification in Cape Verde with the services of implementation, audit, Services, certification, Documentation, Gap analysis and registration process. GLP registration in Cape Verde is very simple, fast, and affordable. You have various choices to do that, for example, you can keep in touch with us on [email protected] or visit www.certvalue.com.  

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We are happy on Certvalue services. The team guided through applicable SOPs, forms and policies to implement QMS and manage it effectively so as to comply with ISO requirements. It included training part as well. Hence we are satisfied and recommend anyone who seek professional service.
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Certvalue team was very professional in their approach from the time we engaged them. Special mention to Ms. Jeevika Uchil who consulted and worked extensively with our team.
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CyberDome Nigeria Limited. CertValue made the acquisition of our ISO 27100 certification seamless. The person assigned to us Jeevika Uchil was very helpful.
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Certvalue is a very professional and responsive consultation firm. It did show us the right direction towards the ISO and GMP certifications for the PPE devices we are manufacturing. Hoping to work with them for ISO 13485 /CE and FDA as well. Well recommended for all.
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We got good service from certvalue and its team I was satisfied,thank you Certvalue for making my work easy
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Thank you certvalue, we have built information security management system in our organization with the help of certvalue. They were really help to get certified under iso 27001. Thank you.
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Very professional in consultation, documentation etc right from the first point of meeting with them. . .thank you certvalue for all the support !
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Certvalue team was very responsive right from the time we contacted them for the first time. Consultants who worked with us were very professional and demonstrated a lot of patience to get us through required documentation / requirments for the certification. Thank you Certvalue!
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