Laura Brown Training
Quality in-house Biopharma Training and QA
Email : Tel : +44(0)1494 873 566
Laura Brown Training
International expertise for in-house customised technical and management skill training, and quality assurance audit for Pharmaceutical, Biotechnology, Medical Device and Healthcare organisations.
About Us
In-House Courses
GCP courses
Data Integrity
Project Management
Technical Pharma
Management and Personal skills
Pharma "mini MBA"
Pharma Leadership skills
Support staff
Training Consultancy/other services
Audit services
Useful Links



Technical Pharma Courses

Laura Brown Training and Development has an outstanding reputation for training R & D personnel, particularly in the area of clinical trial regulations, GCP, pharmaceutical project management, leadership and the pharma mini MBA. We can help you to maximise the R & D professionals’ contribution to the quality of their work in a highly regulatory and GXP compliant environment.

Our emphasis is on the practical application of knowledge and technical and management expertise essential for effective working in the pharma and associated industries. These courses can also help you prepare for potential regulatory inspections.

Examples of the courses include:

Clinical Trials Regulations in the EU

  • Regulatory affairs for clinical trials
  • Regulatory and guideline requirements for clinical trials in the EU
  • Regulatory and guideline requirements for clinical trials in the EU  and US

GCP (Good Clinical Practices) courses

  • ICH GCP  (R2)
  • GCP Update and latest developments
  • GCP overview and refresher
  • overview courses
  • Advanced GCP
  • Courses are available for CRAs/ monitors/ support staff/study site professionals including Investigators/ and courses for specific disciplines including Regulatory Affairs and Pharmacovigilance professionals

Clinical Research courses

  • Training for monitors/CRAs and/or clinical research support professionals
  • Risk based monitoring
  • Effective monitoring visits
  • CRA course for both new CRAs and advanced CRA courses
  • How to write clinical SOPs
  • How to audit
  • How to prepare for inspection/audit
  • Clinical trial regulations and directives
  • Clinical QMS
  • Sponsor Oversight of CROs

Other Pharma Technical courses

  • Clinical Trials Regulations
  • Understanding the pharma industry/Overview of drug development
  • CAPA (corrective and preventative action)
  • Regulatory affairs
  • Data Integrity
  • How to write SOPs
  • Sponsor oversight of vendors
  • QMS
  • Risk Management

Pharma Project Management courses

  • Project management for pharma professionals
  • Project management for clinical research
  • Project management for regulatory affairs
  • Project management for support staff
  • Leadership
  • Team leadership courses
  • Team building sessions

“An excellent overview of product development and the pharmaceutical industry – she knows what she is talking about and provided relevant information customised to our needs, and delivered in an enjoyable way” (Roche).

All courses can be tailored to your specific needs

To find out more about any of these courses or to discuss how a course could be tailored to your specific needs, please contact Laura Brown.