Compliance And Quality Division

Diamond Pharma Services offers GMP and GDP compliance services from clinical development to commercial distribution of the products’ lifecycle.

1. Clinical Trial Phases

  • Contracted QP services for IMP supplies.

2. Marketing Authorisation Submissions

  • API and excipient supplier audits to support QP declarations.
  • Selecting and approving third party analytical testing laboratories.
  • Process and analytical transfers.
  • Selecting and approving third party vendors for contract storage and distribution.
  • Technical agreement generation/review between client and all vendors.

3. Commerical Manufacturing and Distribution

  • Ongoing GMP/GDP Regulatory Compliance Support.
  • GMP/GDP Quality Assurance support.
  • Contracted QP services.
  • Act as contracted RP for MIA holder that has contracted wholesaler distributor.
  • Due diligence audits prior to regulatory audits.
  • Support for GMP training.
 

Case Study

MHRA inspection at overseas client’s manufacturing site:

Diamond Compliance and Quality are pleased to announce the positive outcome of the first on- site GMP regulatory audit, by UK’s Medicines and Healthcare products Regulatory Agency (MHRA), of an overseas client in Bangladesh in July 2017. A representative of Diamond Compliance and Quality undertook a pre-audit readiness gap analysis inspection and subsequently returned to the site during the MHRA audit. The MHRA inspection resulted in no Critical nor any Major observations being raised.

Prior to resumption of formal on-site audits in Bangladesh, by MHRA, Diamond Compliance and Quality had provided support to the same client by liaising with the VMD and MHRA Inspectorate’s Risk, Control and Governance Unit for renew of the expiring VMD GMP certificate and granting of a MHRA GMP certificate following a desktop assessment.






Case Study

ATMP Regulatory Support

The team at Diamond Pharma Services has world class regulatory experience in assisting companies developing advanced therapy medicinal products (ATMPs). Support can be provided for both cell and gene therapy products for Europe and the US.

Case Study

Clinical Trial Application Service

The CTA team at Diamond Pharma Services is integrated into the Regulatory Development Department. The team has extensive experience in CTA activities for a wide range of product types.

Case Study

Compliance And Quality Division

Diamond Pharma Services offers GMP and GDP compliance services from clinical development to commercial distribution of the products’ lifecycle.