Effective Representation When it Matters Most
TALG’s biotech specialties include good manufacturing practices (GMP), venture capital financing, governance issues and more
Comprehensive Regulatory & Compliance Solutions
Professional and knowledgeable counsel for cutting-edge MedTech firms facing IP, FDA, and capital raise challenges
Renew Your Focus on What You Do Best
Leave the legal worries to TALG so you can focus on bringing your products to market
Is your organization spending more time on legal and regulatory issues
than making devices that work?
Too many MedTech products never reach an audience because of regulation and compliance issues, FDA audits, fines, IP litigation and other behind-the-scenes challenges.
You need a partner with the experience to take these problems off of your plate.
Why Do Biotech & MedTech Firms Choose TALG?
Innovative & Proactive
TALG’s outside-the-box thinkers combine experience, practical knowledge, and advanced technology to give clients every edge possible in the boardroom and the courtroom
TALG Knows MedTech
TALG has supported MedTech firms with 510(k) premarket notification submissions, premarket approvals for devices, medical device reporting, Investigational Device Exemptions for clinical studies and much more
Access to capital markets is critical for MedTech firms, and TALG leverages experience in credit transactions, private equity, and equity offerings to produce positive outcomes for our clients
How Do We Get Started?
1) Connect with us and book a meeting
Let’s talk about what you do and how you do it — confidentially, of course
2) Identify your needs and how TALG will help
TALG can provide solutions for your challenges from FDA-to-Z
3) Create a plan of action
We tackle your legal and regulatory obstacles (so you can get back to work)
TALG founder and partner Ismail Amin shared exclusive insights on FDA Device Safety & Reporting Best Practices at DeviceTalks West!