Medicines and Healthcare products Regulatory Agency

Issued following an inspection in accordance with :

Regulation 331A of The Human Medicines Regulations 2012 (SI 2012/1916)

  The competent authority of United Kingdom confirms the following :    

Has been inspected under the national inspection programme in connection with manufacturing authorisation no. UK MIA 17696 in accordance with Regulation 17 of The Human Medicines Regulations 2012 (SI 2012/1916)

From the knowledge gained during inspection of this manufacturer, the latest of which was conducted on 16/12/2020, it is considered that it complies with

• The principles and guidelines of Good Manufacturing Practice laid down in Regulation B17 of the Human Medicines Regulations 2012 (as amended)

This certificate reflects the status of the manufacturing site at the time of the inspection noted above and should not be relied upon to reflect the compliance status if more than three years have elapsed since the date of that inspection. However, this period of validity may be reduced or extended using regulatory risk management principles by an entry in the Restrictions or Clarifying remarks field. This certificate is valid only when presented with all pages and both Parts 1 and 2. The authenticity of this certificate may be verified in MHRA-GMDP. If it does not appear, please contact the issuing authority.

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Operations

1. MANUFACTURING OPERATIONS

[ 1.1 ] Sterile Products

[ 1.1.1 ] Aseptically prepared (processing operations for the following dosage forms)

[ 1.1.1.4 ] Small volume liquids Special Requirements Pathogenic Organisms (Biosafety Level 3 or 4)

[ 1.2 ] Non-sterile products

[ 1.2.1 ] Non-Sterile Products (processing operations for the following dosage forms)

[ 1.2.1.6 ] Liquids for internal use Special Requirements Live Cells

[ 1.2.1.17 ] Other non-sterile medicinal products Manufacture of low bioburden bulk drug substance solutions Special Requirements Live Cells

[ 1.3 ] Biological medicinal products

[ 1.3.1 ] Biological medicinal products

[ 1.3.1.2 ] Immunological products Special Requirements Live Cells

[ 1.3.1.4 ] Gene therapy products Special Requirements Live Cells

[ 1.3.1.5 ] Biotechnology products Special Requirements Live Cells

[ 1.3.1.8 ] Other biological medicinal products Antibodies,Antibody conjugates, Live microbial products, Therapeutic Virus, Plant extracted material Special Requirements Live Cells

[ 1.4 ] Other products or manufacturing activity

[ 1.4.2 ] Sterilisation of active substances/excipients/finished products:

[ 1.4.2.1 ] Filtration

[ 1.4.2.3 ] Moist heat

[ 1.6 ] Quality control testing

[ 1.6.2 ] Microbiological: non-sterility

[ 1.6.3 ] Chemical/Physical

[ 1.6.4 ] Biological

2. IMPORTATION OF MEDICINAL PRODUCTS

[ 2.1 ] Quality control testing of imported medicinal products

[ 2.1.2 ] Microbiological: non-sterility

[ 2.1.3 ] Chemical/Physical

[ 2.1.4 ] Biological

[ 2.3 ] Other Importation Activities

[ 2.3.1 ] Site of Physical Importation

[ 2.3.2 ] Importation of Intermediate which undergoes further processing

Contact Details

26/08/2021	Name and signature of the authorised person of the Competent Authority of United Kingdom
	Confidential
	Medicines and Healthcare products Regulatory Agency
	Tel : Confidential