SEDA CLINICAL MANUFACTURING SERVICES LTD. – MIA(IMP) 59823
| Authorisation Number | UK MIA(IMP) 59823 |
| Category | MIA(IMP) |
| Holder | SEDA CLINICAL MANUFACTURING SERVICES LTD. |
| Registered Address | SEDA CLINICAL MANUFACTURING SERVICES LTD., 5000 LAKESIDE, CHEADLE ROYAL BUSINESS PARK, CHEADLE, SK8 3AX, UNITED KINGDOM |
| Authorisation Date | Jan 22, 2026 |
| Legal Basis | InvestigationalPart 6 of The Medicines for Human Use (Clinical Trials) Regulations 2004 [SI 2004/1031] |
| Sites | 1 |
| Manufacturing Operations | 1.2 1.2.1 1.2.1.1 1.2.1.13 1.2.1.8 1.2.2 1.5 1.5.1 1.5.1.1 1.5.1.11 1.5.1.13 1.5.1.8 1.5.2 1.6 1.6.3 |
| MHRA Link | View on MHRA Website |
Sites (1)
SEDA CLINICAL MANUFACTURING SERVICES LTD.
MANUFACTURING_SITE
Country: UNITED KINGDOMProduct Class: Human Investigational Medicinal Products
Manufacturing
1.2 — Non-sterile investigational medicinal products
1.2.1 — Non-Sterile Products (processing operations for the following dosage forms)
1.2.1.1 — Capsules, hard shell
1.2.1.8 — Other solid dosage forms
1.2.1.13 — Tablets
1.2.2 — Batch certification
1.5 — Packaging
1.5.1 — Primary packaging
1.5.1.1 — Capsules, hard shell
1.5.1.8 — Other solid dosage forms
1.5.1.11 — Semi-solids
1.5.1.13 — Tablets
1.5.2 — Secondary packaging
1.6 — Quality control testing
1.6.3 — Chemical/Physical
Content Preview
The source document is available on KeyPedia. Sign in to view.