Qualified Person
for industrial batch release (Directives 75/319/EEC and 81/851/EEC consolidated within Directives 2001/83/EC and 2001/82/EC). Certification to conformity of investigational medicinal products also available.

  Independent Auditor
of a range of external contractors, such as for analytical results.

  Trainer
in Good Pharmaceutical Manufacturing Practice (GMP) and auditing

  Author
of probably the only 'pharmaceutical' novel: Drugs and Desire

  Speaker
delivering a fresh different speech for that special occasion


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