About PharmOut Consultants

PharmOut Brochure

PharmOut is an international consultancy of professionals working throughout the Asian Pacific region, Australia, China, Hong Kong, New Zealand and South Africa.

PharmOut consults to the pharmaceutical and life science industries.

Our Services

We specialise in Good Manufacturing Practice compliance to the regulations / guidelines issued by PIC/S, HSA, WHO, FDA and TGA.

We offer specialised Good Manufacturing Practice Training courses for your employees to equip them with the necessary skills to be compliant.

Products

We offer Electronic Documentation Management Software (EDMS) product and a number of Training Solutions.

Download the brochure describing our offering.

Our people

PharmOut employs a team of Experienced Pharmaceutical Engineers, GMP Consultants, Validation Consultants, Technical Document Writers. Our staff have an extensive range of experiences which includes the Pharmaceutical, Medical Device and Biotechnology industries.

Our executive team

Trevor Schoerie

  Trevor Schoerie

Trevor has over 20 years experience in the Pharmaceutical & veterinary drugs industry in South Africa. Experience that includes the production of: Final Solid Oral dosage forms and Liquids, Ointments Creams as well Biotech and API (Active Pharmaceutical Ingredients).

Trevor believes strongly in sensible compliance that delivers business results, not just audit success.
 


Bob Tribe


  Bob Tribe

Experienced, communicative, industry professional who has been a key player in the development of the GMP standards and their application internationally.

Bob was previously the Chief GMP Auditor for TGA, Australia  (1980 – 2003) and Chairman of the Pharmaceutical Inspection Cooperation Scheme [PIC/S] (2000 – 2001).

 

GMP GLP Validation ISO 13485 systems GLP, GMP Validation Training Validation Jobs TGA, Medsafe, FDA
 
Validation Master Plans

Technical Document Writer Case Study

 

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