To maintain professional excellence of personnel within our client’s companies and warrant successful project completion, ZM Group provides broad range of educational programs and translation services including Staff Professional Development Courses and Staff Mentoring, In-house Workshop Trainings and Online Training Seminars, Consultations on Project Design and Conduct, Trial and Internal Documents’ Translations. Our inimitable multilingual speakers with impressive work experience in the areas of clinical trials (CT) and Pharmacovigilance (PV) are ready to share their knowledge and skills with your team addressing all their needs.
Sharing Our Knowledge and Skills
Translation, Training and Consulting
In-House and Online Training Seminars
Whether remotely or in the comfort of our client’s office, ZM Group team is ready to deliver high-quality professional seminars and workshops on a variety of pharmacovigilance, regulatory, quality, project management, and clinical trial conduct topics.
- Online Training Seminars
- In-House Workshops
- General courses
- Advanced courses
- Individually-designed courses
- Different group sizes and professional background
- Multilingual
Mentoring and Staff Development
Your goals become our goals. And your success becomes the only true measure of our success. ZM Group offers variety of courses to meet your corporate needs:
- General courses on various industry related topics (GCP, Pharmacovigilance, Quality Assurance, Project Management, Monitoring)
- Advanced courses targeting a specific area (GCP – Good Documentation Practices, Essential Documents Management, Trial Master File. Pharmacovigilance – Individual Case Safety Reporting, Data Safety Monitoring Board, SAE Management)
- Individually-designed courses are available on request to promote client’s team professional growth
Project Design and Conduct
ZM Group is ready to provide general, targeted, and individually-designed approach and step-by-step instructions for a project initiation and high-quality implementation – from Feasibility to Clinical Study Report Development; from Drug Safety Monitoring System establishment to Individual Case Safety Report (ICSR) Forms completion.
Translations
- English, Russian, Chinese (Mandarin)
- Pre-Clinical Trial Documents
- Clinical Trial Documents
- Pharmacovigilance Documents
