We can fill in the gaps in your pharmacovigilance team
When it comes to pharmacovigilance, precision and attention to detail are key. Med Communications, Inc.’s team of highly skilled pharmacovigilance professionals has years of experience covering multiple therapeutic areas in both clinical trials and post-marketing products. Our training programs are comprehensive, supporting client-specific quality updates, product and therapeutic area updates, current laws and regulations, and relevant software updates. Here’s what one of our clients had to say about our pharmacovigilance support services:
“I just wanted to let you know that I’ve had an amazing experience so far with Med Communications and my team from Pharmacovigilance. The pharmacovigilance director has been a superior partner, helping me fill the gaps of my knowledge and not letting anything slip, even if it is about resources coming from our Argus server vendor. The team has been working tirelessly behind the scenes as well to keep everything moving and get questions answered. I’m honestly not sure what I would do without them at this point, and I know for a fact that we wouldn’t be meeting our deadlines if it wasn’t for them.”
—Pharma Company
We offer a full suite of pharmacovigilance services, including:
- Case management
- Literature
- Regulatory reporting
- Risk management
- Signal management
- Regulatory intelligence
- Pharmacovigilance consultancy
Patient safety is the ultimate objective of any pharmacovigilance or drug safety department. The appropriate number of qualified, trained personnel are needed to ensure quality pharmacovigilance processes and outcomes in this rapidly evolving regulatory environment. To learn more about how we can support your PV staff, contact us at 877-477-0977 or https://medcommunications.com/contact-us/.
