Course description
Mastering Regulatory and Development Strategies for Generics - PTI Training Course
Releasing a generic drug on the market can be fraught with regulatory challenges and compliance issues. This training course will allow participants to gain a strategic insight into key requirements for developing generics from a global perspective and an overview of the generics market.
The course covers current trends and practices, and looks at future strategies for regulatory compliance.
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Suitability - Who should attend?
This training programme is aimed at professionals specialising in Regulatory operations within the pharma industry, especially those in the following functions:
- Regulatory Affairs Managers/Officers/ Assistants
- Compliance Managers
- Product Registration Personnel
- Project Managers in Regulatory Affairs
- Documentation Managers
- Key contributors to submission procedures
Why choose PTI
On average, delegates of their online academies said:
Quality of content:
4/5
85% had applied content during the course to their role
Delivery rating:
4/5
Reviews
Expenses
The cost of this training course is £1595 + VAT per participant, which covers tuition and course materials.
In-house Training
PTI - Pharmaceutical Training International can also deliver this course as in-house training for your company. You can reduce costs, enhance accessibility to training resources and better address your company’s own business goals with a tailored PTI training package.
“Discussions were very interesting. The trainer’s performance and course content were great.” Junior Associate for Regulatory Affairs, HALMED