VANESSA ANDERSON

I have 20 years of legal experience and I advise Pharmaceutical and Biopharmaceutical clients and prepare, draft and negotiate a wide variety of Research & Development/Clinical Operations services contracts and Clinical Trial Agreements. I advise clients on Research & Development/Clinical Operations agreements from pre-clinical through post-marketing stages and on the attendant issues including publication, trial registry, human subject research ethics, informed consents, IRB/Ethics Board approvals, subject injury, ICH GCP compliance, privacy, financial reporting and pre-clinical research ethics. I also have extensive experience in conducting in-licensed approved and new drug product integration and transition and in preparing all necessary contractual transfers and attendant transition processes... Vanessa Hamilton Anderson is an Attorney/Consultant in the field of Clinical Trials Contracting/Regulatory Compliance at VRH Anderson, PLLC

Also known as: VRH Anderson, PLLC