GMP Certification in Ethiopia

Certvalue is one of the leading GMP Consultants in Ethiopia for providing GMP certification in Ethiopia, Addis Ababa, Dire Dawa, Harar, Mekele and other major cities in Ethiopia with the services of implementation, Documentation, Audit, Templates, Training, Gap Analysis, Registration at affordable cost to all organization to get Certified under Good Manufacturing Practice Management System in Ethiopia. GMP Certification in Ethiopia is used for good Manufacturing Practice (GMP) is a term that is recognized Globally for the control and management of manufacturing, testing the overall quality control of food and pharmaceutical products. GMP addresses a subject issue including documentation, recording information, qualifications, sanitation, cleanliness, equipment verification, validation process, and complaint handling. All most all GMP requirements are very general and open-ended, allowing each manufacturer to decide the best necessary controls. the quality approach of GMP Consulting Services in Ethiopia secures manufacturing, enabling companies to minimize contamination, mistakes, and errors. This, in turn, protects the customer from purchasing a product, which is not effective or dangerous. GMP registration in Ethiopia is a system to make sure that products are always produced and controlled according to quality standards. It is designed to minimize the risks complex in any pharmaceutical production that cannot be eliminated through testing the final product. Requirements of GMP Certification in Ethiopia:
  • Good documentation makes up a necessary part of the quality assurance system. Written policy prevents errors resulting from spoken communication, and clear documentation authorize tracing of activities performed.
  • form must be designed, prepared, reviewed, and distributed with care.
  • Documents must be approved, signed, and dated by the suitable competent and authorized persons.
  • Documents must have distinct contents. The title, nature, and purpose should be distinctly stated. They must be laid out in a well-ordered fashion and be easy to check the reproduced documents must be clear and legible.
  • Documents must be regularly reviewed and kept updated. When a document has been revised, systems must be operated to prevent accidental use of superseded documents (Example only current documentation should be accessible for use).
  • Documents must not be handwritten; however, documents require the entry of data, these entries may be made in understandable legible handwriting using a suitable indelible medium (i.e., not a pencil). Enough space must be provided for such entries.
The following GMP Certification in Addis Ababa approach concern ‘documentation and records’ may be helpful for pharmaceutical manufacturers to meet the assumption of different regulatory organizations. Write good procedures and follow them, think what has happened in a workspace if written procedures are not available. People depend on more senior employees to tell them how to do things and then do their job. This is exceptional for an organization making garden pots, but not so good when the products being made are pharmaceuticals and can even cause death! Figure the task before you begin writing the procedure. Create a brief crash of the important steps and key points related to the task.  Following procedures, it is all very well to have a great written plan of action in place but to ensure a controlled and compatible performance they need to be followed; it is a GMP requirement. Often, the steps described in a written policy may not be appear to the most efficient way of working, and taking shortcuts may save time. These are the two main reasons for this:
  • Many shortcuts may create a risk that can be expensive in the end.
  • Each step in a procedure has been covered for a purpose.
Keep good records, Good records allow one to track all activities performed during batch manufacture, from the getting of raw materials to the final product release; they come up with a history of the batch and its distribution.

Benefits of using GMP Certification Services in Ethiopia?

Benefits for the manufacturer one of the main benefits is remarkably improved quality systems and quality agreement at the excipient manufacturer. We have seen these improvements in the months leading up to GMP certification and carry on with during the years immediately following GMP certification. Some excipient mass producers were already at a high level of GMP compliance and certification. Benefits of GMP Certification Services in Ethiopia GMP Services in Ethiopia Enhances the food safety management system. GMP Consultants in Ethiopia Increases Clients trust in your products GMP Certification Cost in Ethiopia Helps to decrease operating costs due to rework and penalties due to non-compliance GMP in Ethiopia Helps boost export opportunities. Reduced duplication of inspections Which industries eligible for GMP Certification in Ethiopia?
  • Manufacturing Companies
  • Pharmaceuticals Companies
  • Food Manufacturing Companies.

How to get GMP Consulting Services in Ethiopia?

Certvalue is providing GMP Certification Services in Ethiopia with extensive expertise and experience in all International food and pharmaceutical products Standards. For GMP Certification in your organization, reach Certvalue – GMP Consultants us at +776017362326 Send your requirements to Our experts will call you and guide for Successful GMP Certification in Ethiopia. We would be happy to assist your company in the GMP Certification process in Ethiopia to send your research after contact

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


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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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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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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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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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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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