Why You Need to Take This Training Course?
This Course will :
1. Boost Your Career Prospects:
- Increased Expertise: The course equips you with the knowledge and skills to prepare data dossiers for veterinary pharmaceuticals, making you a valuable asset to animal health companies.
- Stand Out from the Crowd: In a competitive job market, this specialized training can set you apart from other candidates.
- Higher Earning Potential: Your newfound expertise could lead to promotions or opportunities in higher-paying positions.
2. Ensure Regulatory Compliance:
- Confidence in Dossier Preparation: The course provides a clear understanding of the regulatory requirements for veterinary drug submissions, ensuring your dossiers meet all necessary standards.
- Reduced Risk of Delays: Proper dossier preparation minimizes the chances of your submissions being rejected by regulatory agencies, saving time and money.
- Peace of Mind: Knowing you’ve prepared compliant dossiers gives you peace of mind and allows you to focus on bringing new veterinary treatments to market.
3. Maximize Efficiency with Upbeat Consultations:
- Personalized Guidance: The upbeat consultations provide an opportunity to ask questions and get tailored advice from experienced professionals, ensuring you grasp complex topics effectively.
- Clear Communication: The positive and encouraging atmosphere fosters clear communication, making the learning process more engaging and enjoyable.
- Time-Saving Support: Upbeat consultations can help you troubleshoot challenges and avoid common mistakes, saving you valuable time and effort.
What you'll learn
- Participant will have general introduction on the overall structure of the Veterinary dossier data information requirements
- Participant will understand how to fill & review part one of the Vet file based on ICH guidelines (ex. using SFDA & Gulf Requirements) with examples
- Participant will be able to compile and/or evaluate registration part two (Quality Documentation) of the Vet file to insure submission without deficiencies. This will be supported with examples
- Participant will understand the different studies (safety and residues tests , preclinical and clinical trials) needed to complete part three and four of the file and the rational behind them
Instructor: Dr. Samer Sowidan
This 15-hour Training Course is Equivalent to 13 Continuing Professional Development (CPD) hours.
- Duration: 15 Hrs. Two Days
- Time: 9.00 am-4.30 pm
- Prerequisite for this course: None
- Language: English
- Level: Management or any one interested
- Classroom or Vitual Training
- Price US $ 495
- Certified and Accredited Certificate
- Discount available for companies who send three or more participants
- Seats for this course: 12
- Virtual through google meet
- Classroom course at Upbeat office, hotel or at the customer premises
