Top of the Class
In the modern life science sector, regulatory standards have never been higher. This means the need for well-trained industry professionals is at a premium. You need your staff to be informed, knowledgable, and ready to make quality conscience and compliant decisions.
Our twenty-week Quality Assurance Accreditation Program is designed to give professionals new to pharmaceuticals, medical devices, and biologics the tools they need to succeed in complex regulatory markets.
Program Overview
Training Materials: Approximately 20 training e-booklets.
Weekly assignments and preparation of questions.
Weekly one-hour coaching sessions by telephone.
E-mail support.
Multiple choice final examination. Passing grade >/= 80%.
Accreditation Certificate issued with one-year expiration date.
Class Benefits
Employees develop skills needed necessary to make quality conscience and compliant decisions.
Cost-Effective. Significantly less than sending employees off-site; saves travel and hotel costs.
Educationally Impactful. Employees are not bombarded with too much information at one time. The weekly format allows students to prepare and maximize each session.
Accreditation of employees demonstrates organizational commitment to excellence.
Fulfills GMP training requirement (21 CFR 211.25).
Audit Option
Significantly enhance the effectiveness of the training for your employees in your particular setting.
Includes a one-day visit to your facility to meet with the trainee(s), assess and audit their working environment, understand the types of challenges they may face with their day to day responsibilities.
The audit can occur before or during the 20-week training period.
Please note: there is an additional charge for the audit option.