Medicines and Healthcare products Regulatory Agency
1: Authorisation Number | UK MIA(IMP) 42803 |
---|---|
2: Name of authorisation holder | TC BIOPHARM LIMITED |
3: Address(es) of manufacturing site(s) |
TC BIOPHARM LIMITED - CLINICAL MANUFACTURING FACILITY, MAXIM 1, 2 PARKLANDS WAY, HOLYTOWN, MOTHERWELL, ML1 4WR, UNITED KINGDOM |
4: Legally registered address of authorisation holder | TC BIOPHARM LIMITED, MAXIM 1, 2 PARKLANDS WAY, HOLYTOWN, MOTHERWELL, ML1 4WR, UNITED KINGDOM |
5: Scope of authorisation and dosage forms | ANNEX 1 and/ or ANNEX 2 |
6: Legal Basis of authorisation | |
7: Name of responsible officer of the competent authority of the member state granting the manufacturing authorisation | Confidential |
8: Authorisation Date | 18/03/2024 |
9: Annexes attached | Annex 1 and/or Annex 2 |
SCOPE OF AUTHORISATION
Annex 2
Name and address of the site:
TC BIOPHARM LIMITED - CLINICAL MANUFACTURING FACILITY, MAXIM 1, 2 PARKLANDS WAY, HOLYTOWN, MOTHERWELL, ML1 4WR, UNITED KINGDOM
Human Investigational Medicinal Products
Authorised Operations |
MANUFACTURING OPERATIONS (according to part 1) |
Part 1 - MANUFACTURING OPERATIONS |
[ 1.1 ] Sterile Investigational Medicinal Products |
[ 1.1.1 ] Aseptically prepared (processing operations for the following dosage forms) |
[ 1.1.1.4 ] Small volume liquids Special Requirements Live Cells |
[ 1.1.3 ] Batch certification |
[ 1.3 ] Biological investigational medicinal products |
[ 1.3.1 ] Biological medicinal products |
[ 1.3.1.3 ] Cell therapy products Special Requirements Live Cells Cell Banking |
[ 1.3.2 ] Batch certification |
[ 1.3.2.3 ] Cell therapy products Special Requirements Live Cells Cell Banking |
[ 1.5 ] Packaging |
[ 1.5.2 ] Secondary packaging |
[ 1.6 ] Quality control testing |
[ 1.6.1 ] Microbiological: sterility |
[ 1.6.2 ] Microbiological: non-sterility |
[ 1.6.3 ] Chemical/Physical |
[ 1.6.4 ] Biological |