Because pharmaceutical sales reps work in a highly technical, regulated industry, the training materials they use have to pass a stringent review process first. This process is called the Medical Legal Regulatory (MLR) or Promotional Review Committee (PRC). It ensures any promotion of a pharmaceutical product is medically accurate and complies with the regulations of the Food and Drug Administration (FDA) and any other applicable laws and regulations. Reviewers are experts in regulatory matters, legal issues, and medical affairs, and they ensure training is compliant in every respect.
The key to creating pharmaceutical sales training material that clears all these hurdles is a good working relationship between project managers and reviewers and an attitude on everyone’s part that everyone’s views should be heard. If you’re developing training materials, here are some ways to help smooth the MLR process.
Envision the Material from the Learner’s Point of View
Before submitting a piece of training material for review, think about how it fits into your training program. Training must be thorough, but if your review team knows that the bit you’re submitting is only one of several modules to come, it can prevent them from overzealously adding to the material. Let reviewers know, for example, that this particular module is designed to explain one aspect of training (such as the emotional impact a medical condition can have), and that other training modules headed for the review cycle provide all the factual knowledge that goes along with it.