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General GMP Services
for the
Pharmaceutical and Biotechnology Industries
What can MEC do for your company?
Our Quality Advisors can assist you with the following:
Manufacturing
- Facility Upgrade to CT Directive
- Contract Manufacture
Regulatory Affairs
- Chemistry & Pharmacy (Quality / CMC dossier)
- Common Technical Documents
- Dossier Audits
Management of Change
- Change Control
- Technology Transfer
Training
- Basic GMP
- Manufacturing
- Quality Control
- Customised Quality Training to specific needs
- Quality Systems
- Clinical Trial Supplies, Design, Preparation & Distribution
GAP Analysis
- Quality Systems
- GMP Standards
- Quality Control Standards
- Training
- Management of Change
- Auditing Services
Clinical Trial Supplies
- Strategy for Design and Provision of Clinical Trial Supplies.
- Contractors — Audit & Management
- Packaging
- Labelling
- Logistics
- Randomisation & Blinding
- IVRS
Looking for Additional Information?
Why not call us for an informal chat?
Marilyn Emery Consulting
33 Enterprise House
Springkerse Business Park
STIRLING
FK7 7UF
Scotland
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Tel:
Fax:
Email:
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+44 (0) 1786 445 777
+44 (0) 1786 849 269
info@marilynemery.com |
Those acronyms decoded:
| GCP | Good Clinical Practice |
| GDP | Good Distribution Practice |
| GLP | Good Laboratory Practice |
| GMP | Good Manufacturing Practice |
| IMP | Investigational Medicinal Products |
| QA | Quality Assurance |
| QP | Qualified Person |
| UK | United Kingdom |
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