pharmitas.co.uk

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Reliable Technical Assistance for the Pharmaceutical Industry. Limited can provide flexible, cost-effective support in the areas of Regulatory Affairs (especially biological and biotechnology products), Quality Assurance, QP batch release, Responsible Person duties, auditing, training, and Code of Practice compliance. If you are looking for on-going technical assistance or for immediate project execution in any of the above areas Pharmitas. May be able to help you.

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Pharmitas Home | pharmitas.co.uk Reviews

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Reliable Technical Assistance for the Pharmaceutical Industry. Limited can provide flexible, cost-effective support in the areas of Regulatory Affairs (especially biological and biotechnology products), Quality Assurance, QP batch release, Responsible Person duties, auditing, training, and Code of Practice compliance. If you are looking for on-going technical assistance or for immediate project execution in any of the above areas Pharmitas. May be able to help you.

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Pharmitas Home | pharmitas.co.uk Reviews

https://pharmitas.co.uk

Reliable Technical Assistance for the Pharmaceutical Industry. Limited can provide flexible, cost-effective support in the areas of Regulatory Affairs (especially biological and biotechnology products), Quality Assurance, QP batch release, Responsible Person duties, auditing, training, and Code of Practice compliance. If you are looking for on-going technical assistance or for immediate project execution in any of the above areas Pharmitas. May be able to help you.

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pharmitas.co.uk

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Pharmitas Home

http://pharmitas.co.uk/why.html

Reliable Technical Assistance for the Pharmaceutical Industry. Technical or regulatory advice when starting up in the UK. An extra pair of hands to assist with a large regulatory project. The services of a QP or Responsible Person. Specialist biological or biotech product expertise. Assistance to meet your auditing commitments. To contain your fixed costs. What Pharmitas can provide for you:. A pragmatic and knowledge-based approach. RP and QP services including batch release.

2

Pharmitas Home

http://pharmitas.co.uk/profile.html

Reliable Technical Assistance for the Pharmaceutical Industry. Jon Betts is a registered pharmacist with over 30 years experience in the pharmaceutical industry. He began his career at Pfizer, Sandwich working in Pharmaceutical R and D before moving to Glaxo Operations, Barnard Castle and then Rhone-Poulenc, Dagenham. He has gained considerable production experience in the manufacture of tablets, sterile products, creams and ointments and is eleigible to act as a Qualified Person. Jon is respected intern...

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Pharmitas Home

http://pharmitas.co.uk/index.html

Reliable Technical Assistance for the Pharmaceutical Industry. Limited can provide flexible, cost-effective support in the areas of Regulatory Affairs (especially biological and biotechnology products), Quality Assurance, QP batch release, Responsible Person duties, auditing, training, and Code of Practice compliance. If you are looking for on-going technical assistance or for immediate project execution in any of the above areas Pharmitas. May be able to help you.

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bioreg-advice.de

BioReg Consultancy - Management Consultancy for biopharmaceutical companies: Network

http://www.bioreg-advice.de/network.html

BioReg Consultancy’s international network of experts comprises:. With the main focus on development, regulatory affairs and GMP inspections for biopharmaceuticals. Pauels Consulting, Germany. With the main focus on nonclinical development of biopharmaceuticals. Pharmitas Ltd, Jon Betts, United Kingdom. With the main focus on UK manufacturing and QP batch release. Archemin bvba, Belgium. With the main focus on regulatory affairs in the Benelux region. Judy Atkins, USA.

bioreg-advice.com

BioReg Consultancy - Management Consultancy for biopharmaceutical companies: Network

http://www.bioreg-advice.com/network.html

BioReg Consultancy’s international network of experts comprises:. With the main focus on development, regulatory affairs and GMP inspections for biopharmaceuticals. Pauels Consulting, Germany. With the main focus on nonclinical development of biopharmaceuticals. Pharmitas Ltd, Jon Betts, United Kingdom. With the main focus on UK manufacturing and QP batch release. Archemin bvba, Belgium. With the main focus on regulatory affairs in the Benelux region. Judy Atkins, USA.

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Reliable Technical Assistance for the Pharmaceutical Industry. Limited can provide flexible, cost-effective support in the areas of Regulatory Affairs (especially biological and biotechnology products), Quality Assurance, QP batch release, Responsible Person duties, auditing, training, and Code of Practice compliance. If you are looking for on-going technical assistance or for immediate project execution in any of the above areas Pharmitas. May be able to help you.

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