Online Fax for Pharmaceutical Manufacturers & Life Sciences
Pharmaceutical manufacturers operate under among the most rigorous documentation requirements of any industry — FDA submissions, clinical trial documents, batch manufacturing records, and drug labeling documents must be transmitted to regulators, clinical sites, and CMOs with precise documentation and audit trails. FDA facility inspections and NDA reviews expect complete, dated records of all regulatory communications.
Common Documents
Compliance
Pharmaceutical manufacturers must comply with FDA's 21 CFR Parts 210 and 211 for current Good Manufacturing Practices, and 21 CFR Part 11 for electronic records and signatures. Clinical trial sponsors must comply with ICH E6 GCP guidelines. Send FAX Mail's timestamped transmission records support GMP documentation requirements for batch record and regulatory communication audit trails. Manufacturers should validate electronic fax records for 21 CFR Part 11 compliance where applicable.
Starter
- 600 fax pages per month
- 1 dedicated fax number
- Send & receive faxes
- Fax to email delivery
- Fax history & downloads
- No per-page overage charges
Professional
- 2,000 fax pages per month
- 3 dedicated fax numbers
- HIPAA compliance
- Send & receive faxes
- Priority delivery
- No per-page overage charges
Business
- 5,000 fax pages per month
- 5 dedicated fax numbers
- HIPAA compliance
- Audit logs
- Team roles & permissions
- Priority support
Enterprise
- 8,000 fax pages per month
- 10 dedicated fax numbers
- Everything in Business
- API access
- Dedicated support
- Custom integrations
No per-page overage. No activation fees. No contracts. Cancel anytime.
Pharmaceutical Fax — FAQ
Modernize your pharmaceutical fax workflow
Send your first fax free. No credit card required.
Start Free