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+254 718 353235

cGMP Training &

GMP AUDITS / INSPECTIONS

Prescription Drugs

ENSURING THE HIGHEST standard

Frequently, cGMP compliance issues are triggered by non-conformance to regulatory commitments. Dolian International will provide you with QA/cGMP consulting services to ensure compliance with WHO - GMP.

 

You will receive professional services such as

  • How to set up a GMP compliant pharmaceutical company, Quality Systems,

  • (PQS),

  • PIC’s GMP standards,

  • conducting GMP audits,

  • GMP Training,

  • Documentations,

  • Batch record review,

  • GMP batch release and

  • Support for pre-approval inspections (PAI).

QUALITY AND COMPLIANCE CONSULTING

We will help you achieve cGMP compliance in all aspects of 

  • Production,

  • Documentation,

  • Premises,

  • Equipment,

  • Materials,

  • Personnel,

  • Quality control,

  • Contract manufacturing and analysis,

  • Self-insulation,

  • Validations,

  • Complaints & recalls. 

our services include

  • ​Design and implementation of GMP Quality Systems

  • GMP audits / GMP Training

  • GMP Documentation review

  • PAI-readiness assessment/Support

  • CMO Oversight (person-in-the-plant)

  • GMP investigations and deviation reports

  • Product complaints and product recalls

   Request  A CONSULTATION

Dolian brings over twenty years of experience to the goal of providing pharmaceutical companies with an unparalleled level of service and dedication to ensure the success of their business.

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P.O BOX 683 - 00618

Ruaraka, Nairobi- Kenya

Tel: +254 718 353235

Opening Hours: 9am - 7pm

© 2025 Dolian International Limited. Proudly created by Dorine Ogutu

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