by MVG Consulting | Oct 28, 2019 | Clinical Trials
We provide companies alternatives to the large contract research organizations, helping small to medium sized biotechnology and pharmaceutical companies with their clinical development programs.
by MVG Consulting | Oct 17, 2019 | Clinical Trials
–Full Standard Operating Procedures (SOPs) –Study & site startup activities –Documents and Submissions –IRB/EC meeting activity –Contracts & budgets –Screening and enrollment –Study subject activity throughout the trial –Regulatory documents (electronic and... by MVG Consulting | Oct 14, 2019 | Industry News
Exciting news for Lupus Nephritis from the FDA. Discover the latest news about our company, our products, our policies, and our people. Source: Genentech: Press Releases | Tuesday, Sep 17, 2019
by MVG Consulting | Oct 7, 2019 | Clinical Trials
Our knowledgeable and multilingual CQA (clinical quality assurance) auditors are well versed in local, national and international regulations, standards and guidelines.
by MVG Consulting | Oct 1, 2019 | Featured
Are you a Clinical Trial Manager, Clinical Project Manager, or Medical Writer looking for your next career move? Contact MVG today with job inquiries! LEARN MORE
