Manufacturing Practice Update for producing Biopharmaceutical Products

Online Training Id: GPP-040

Credits: 4



GBP 250.00

GBP 250.00

The recent demand on Pharma Companies to urgently produce an effective Covid-19 vaccine has required they apply the latest digital technology to current knowledge of the genomic structure of the virus , to ensure that the newly developed vaccine is produced in accordance with the appropriate Manufacturing Practice standards to ensure that the finished vaccine is compliant with the required specification to ensure the efficacy of the new vaccine.  This course will detail the latest developments and techniques of Biotech production and provide an overview of current activities in genomics, in their translation into new drug that can deliver effective treatment.

The recent demand on Pharma Companies to urgently produce an effective Covid-19 vaccine has required they apply the latest digital technology to current knowledge of the genomic structure of the virus , to ensure that the newly developed vaccine is produced in accordance with the appropriate Manufacturing Practice standards to ensure that the finished vaccine is compliant with the required  specification to ensure the efficacy of the new vaccine. 

This course will detail the latest developments the techniques of Biotech production and provide an overview of current activities in genomics, in their translation into new drug discovery and the delivery of personalized medicine.

Credits: 4 CPD / CME

No. of Hours: 4 hrs

Learning Objectives: 

This eLearning Course will provide an overview of the following.

  • The Manufacturing Practice standards required to produce the new generation of Covid vaccine Biopharmaceuticals.
  • Use of Deep Learning in assessing the Pharmacogenomics when developing modern Biopharmaceutical Medicines.
  • Properties of Biopharmaceuticals .
  • The Biotechnology Manufacturing Process
  • Development of the Covid-19 vaccine
  • The facts about Bioequivalence of Biosimilar products

Who Should Enroll:

Pharmacists and Pharmaceutical Scientists needing to know about the development in Pharmaceutical Standards for the manufacture of Biopharmaceuticals


John Dr Jolley  FR PHARM S, FCQI CQP

Is a Pharmaceutical Consultant providing technical consultancy and bespoke training solutions to the Pharmaceutical Profession, he has a degree in Pharmacy and has been awarded fellowships with the Royal Pharmaceutical Society and Chartered Quality Institute as a consultant lead assessor.

I obtained a BSc Pharm Hons degree in Pharmacy, and a research fellowship at Boots research Nottingham working on formulation development, during which time I published several technical papers.

I joined Beecham Products UK as a management Trainee and was later appointed General Manager of a Beecham subsidiary in Ireland, returning to Beecham Head Quarters in London, where I worked as special products adviser to the Divisional Managing Director for Beecham Products.

I was invited to join Boehringer Ingelheim (UK) Ltd as Technical Director and remained there for 15 years before leaving to establish “Pharma Consult” an International technical and training consultancy working with associates in the US- Latin America- Asia Specific, Saudi Arabia and Other GCC countries, and India.
I have held positions with responsibility for; Clinical Research, Product Registration, Manufacturing, Distribution, Quality Assurance, and General Management, and am a practicing Qualified Person (QP) with experience if working in Biotech industry.

I was awarded Fellowship with the Royal Pharmaceutical Society (UK) and in 2003 was elected to serve on the council of the RPS(UK) as their treasurer. In 1998 I became Consultant Lead assessor of the Chartered Quality Institute and in 2015 was invited to join the worshipful Society of Apothecaries and granted the freedom of the City of London


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Online Training Highlights
Duration: 4 hrs
Released On: 09/21/2021
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