Consultancy Services
These can be flexible and will be tailored to your needs. Services can range from a contract for a fixed period of time per week, to a flexible ad hoc arrangement. Work can be done as required e.g. using electronic approval systems such as Zinc maps, or on-site as required for compliance/audit services, or handling of Code enquiries by telephone, post and/or email.
Consultancy services specialise in the following areas:
SOPs, Process Implementation and Audit
• Writing Global, European and UK standard operating procedures on
areas such as the Review and Approval of International Promotional Materials.
• Developing policies on pharmaceutical industry activities such as
Advisory Boards or Company-Organised Meetings, Donations and Grants, and
relationships with Patient Organisations.
• Setting-up and implementing Code Review Processes throughout Europe
and Globally.
• Compliance audit.
Review of promotional material and activities
• Regulatory review of promotional and non-promotional
materials and activities.
• Review of promotional and non-promotional materials for compliance
with the ABPI or EFPIA Codes of Practice.
• Advice on the interpretation of Industry Codes of Practice.
Code of Practice Complaints
- Initiating and responding to Code of Practice complaints
Training
- Lectures and workshops on ABPI and EFPIA Codes of Practice