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Woodley BioReg Regulatory Affairs, Compliance and Conformance for pharmaceutical, biopharmaceutical, healthcare, API and Medical device manufacturers

Woodley BioReg helps pharmaceutical, biopharmaceutical, healthcare, active pharmaceutical ingredient manufacturers and medical device companies develop and manufacture quality products that are effective and safe for patients worldwide.

http://www.woodleybioreg.com/

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Woodley BioReg Regulatory Affairs, Compliance and Conformance for pharmaceutical, biopharmaceutical, healthcare, API and Medical device manufacturers | woodleybioreg.com Reviews

https://woodleybioreg.com

Woodley BioReg helps pharmaceutical, biopharmaceutical, healthcare, active pharmaceutical ingredient manufacturers and medical device companies develop and manufacture quality products that are effective and safe for patients worldwide.

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1

Vacancies

http://www.woodleybioreg.com/join-us.html

T 44 (0)1484 434343. Drug or Device Discovery. Development of Validation Master Plans. Development of QA Systems. Drug or Device Discovery and Development. Short and long-term Project work available for Bio-Pharmaceutical / Medical Device Professionals. Permanent and project specific opportunities are available / considered. We suggest that all candidates apply directly to WBR Ltd. Please only contact us if we have an existing arrangement in place with you. West Yorkshire, UK. Vat No. 790214049.

2

Sector : API Manufacture

http://www.woodleybioreg.com/2011-08-02-20-03-30/api-manufacture.html

T 44 (0)1484 434343. Drug or Device Discovery. Development of Validation Master Plans. Development of QA Systems. Drug or Device Discovery and Development. Sector : API Manufacture. The Active Pharmaceutical Ingredient (API) industry supplies pharmaceutical. LEGISLATION IN API MANUFACTURING. The intermediate manufacturer and the pharmaceutical industry share the same governing bodies, the ( Food and Drug Administration. FDA) in the US, the Medicine and Healthcare Product Regulatory Agency. Based around t...

3

Sector : Healthcare / Over-the-counter Medicines

http://www.woodleybioreg.com/2011-08-02-20-03-30/healthcare-otc.html

T 44 (0)1484 434343. Drug or Device Discovery. Development of Validation Master Plans. Development of QA Systems. Drug or Device Discovery and Development. Sector : Healthcare / Over-the-counter Medicines. And product licence maintenance. The global governing bodies ( Food and Drug Administration. FDA) in the US, the Medicine and Healthcare Product Regulatory Agency. MHRA) in the UK, the Pharmaceuticals and Medical Devices Agency. PMDA) in Japan, and the European Medicines Agency. EMA) for over the count...

4

Method Scouting

http://www.woodleybioreg.com/drug-or-device-discovery-and-development/method-scouting.html

T 44 (0)1484 434343. Drug or Device Discovery. Development of Validation Master Plans. Development of QA Systems. Drug or Device Discovery and Development. Drug or Device Discovery and Development. Method Scouting is the early assessment of potential test methods conducted during the early stages of product development, when there is limited knowledge of the types of analytical procedures. That may be applicable to the product. Method Scouting and Pharmaceutical Development. WBR has expertise and experie...

5

Analytical Development

http://www.woodleybioreg.com/drug-or-device-discovery-and-development/analytical-development.html

T 44 (0)1484 434343. Drug or Device Discovery. Development of Validation Master Plans. Development of QA Systems. Drug or Device Discovery and Development. Drug or Device Discovery and Development. Pharmaceutical and healthcare products require a detailed analysis (chemically, biochemically, and preclinical assessments) as part of the license submission. Analytical tests can be simple and cheap to perform. Analytical methods are well understood and relatively easy to validate. Types of tests are :-.

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A&E Cameron Ltd - Regulatory Affairs Consulting Services

http://www.aecameron.co.uk/consultants.html

Regulatory Affairs Consulting Services. Flexible, innovative, focused on quality and delivery. Aneeta Cameron - Director. A Regulatory Affairs Professional, qualified pharmacist and a Ph.D., with 10 years International Regulatory Affairs experience, in both ethical and consumer products, gained largely through working in blue chip pharmaceutical companies. A&E Cameron has strong links with a number of selected consultants with whom we can provide comprehensive regulatory and quality consulting services.

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Woodley BioReg Regulatory Affairs, Compliance and Conformance for pharmaceutical, biopharmaceutical, healthcare, API and Medical device manufacturers

T 44 (0)1484 434343. Drug or Device Discovery. Development of Validation Master Plans. Development of QA Systems. Woodley BioReg Limited are Regulatory and Quality experts to the healthcare industry. Woodley BioReg helps pharmaceutical, biopharmaceutical, healthcare, active pharmaceutical ingredient manufacturers and medical device companies develop and manufacture quality products that are effective and safe for patients worldwide. Woodley BioReg can help companies manage Registration Drift. WBR now off...

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