I will draft a sec compliant reg d ppm for your biotech startup
Licensed US Attorney Premium Corporate and Healthcare Securities
About this Gig
Raising capital for a biotech startup involves unique regulatory and financial hurdles. Sophisticated investors expect to see a Private Placement Memorandum (PPM) that thoroughly addresses intellectual property rights, clinical trial timelines, research and development (R&D) risks, and SEC compliance.
As a licensed U.S. attorney (Bar No. #37934), I draft premium, SEC-compliant Reg D (506b/506c) PPMs specifically tailored to the biotechnology sector. I do not use generic templates; I meticulously craft your offering documents to reflect the specific scientific, financial, and regulatory realities of your venture.
What you receive:
- Executive Summary & Offering Terms
- Use of Proceeds & Dilution Provisions
- Strict Biotech & Clinical Trial Risk Factors
- Management & Cap Table Disclosures
- SEC Reg D Compliance Structuring
Your documentation must be bulletproof to protect you from liability and demonstrate high-level professionalism to prospective angel investors and venture capitalists. Please send me a message with your biotech startup's details to begin.
Field of law:
Finance
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Business (corporate)
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Commercial
Legal consulting Gigs are not screened
Please note that there is no screening process for this service. We recommend that you message the freelancer and check all necessary details before placing your order. Pro freelancers in this category have gone through a vetting process. You can find more details here.
FAQ
Do you cover both Rule 506(b) and 506(c) offerings?
Yes, I can draft your PPM for either a 506(b) (friends/family/existing network) or 506(c) (public solicitation to accredited investors) offering.
What information do you need from me to start?
I will need your pitch deck, business plan, financial projections, and corporate formation documents. I will review these via Fiverr messages.
Does this include the filing of Form D?
This gig covers the comprehensive drafting of the PPM and investor documents. State/Federal filings are separate.
Are clinical trial risks included?
Absolutely. Biotech requires highly specific risk factors regarding FDA phases, trial failures, and R&D delays, which I will draft.
Is this gig suitable for pre-seed startups?
Yes, whether you are raising an initial pre-seed round or a Series A, I will tailor the legal language to your exact funding stage.
