Pharmaceutical Solutions

Prescription-Strength Email Signatures for Pharma Professionals

Pharmaceutical companies face stringent communication requirements from the FDA, EMA, and global regulators. Siggly helps your teams maintain GMP-compliant signatures with proper disclaimers, credential displays, and adverse event reporting links.

120+
Pharma organizations
99%
Disclaimer compliance
<15 min
Global deployment

Pharma-Grade Signature Management

FDA & EMA Regulatory Fields

Include NDA/ANDA numbers, EMA marketing authorization references, and regulatory affairs contact details that auditors and partners need.

GMP Compliance Badges

Display current Good Manufacturing Practice certification status, facility registration numbers, and DEA schedule details where applicable.

Adverse Event Reporting Links

Automatically include MedWatch reporting links and pharmacovigilance contact information in all outward-facing signatures as required by FDA guidance.

Promotional Review Compliance

Ensure signatures used by commercial teams comply with OPDP guidelines by restricting unapproved claims and including required fair-balance references.

Multi-Market Localization

Manage signature variations for US, EU, APAC, and LATAM markets with region-specific regulatory disclaimers, languages, and local affiliate branding.

Get Your Pharma Team on Siggly

01

Configure Compliance Rules

Set up mandatory disclaimer blocks, adverse event links, and credential fields that must appear on every signature across your organization.

02

Build Department Templates

Create distinct templates for R&D, regulatory affairs, commercial, medical affairs, and manufacturing teams with role-appropriate content.

03

Deploy with Audit Trail

Push signatures globally with full version history and audit logging to satisfy FDA and EMA inspection requirements.

Pharma Teams Using Siggly

Regulatory Affairs

Signatures with NDA numbers, FDA contact references, and submission tracking links for seamless regulator communication.

Medical Science Liaisons

Credential-rich signatures featuring MD/PharmD degrees, therapeutic area specialties, and publication links.

Commercial & Sales

Compliant promotional signatures with fair-balance language and approved product messaging.

Pharmacovigilance

Signatures with mandatory MedWatch links and adverse event reporting instructions for patient safety compliance.

"During our last FDA inspection, auditors asked how we enforce adverse event links in employee emails. We showed them Siggly and they were impressed that every signature was automatically compliant."

Dr. Naveen Gupta

VP of Pharmacovigilance, Alder Biosciences

Frequently Asked Questions

Can Siggly enforce mandatory disclaimers for pharma?
Yes. Administrators can lock disclaimer blocks so they cannot be removed or edited by individual employees, ensuring every email meets regulatory requirements.
How do you handle promotional review compliance?
Siggly supports approval workflows where medical-legal-regulatory teams can review and approve signature content before it goes live, preventing unapproved promotional claims.
Can we include adverse event reporting links?
Yes. MedWatch URLs, pharmacovigilance email addresses, and adverse event phone numbers can be added as mandatory fields that appear on all outward-facing signatures.
Does Siggly maintain an audit trail?
Yes. Every signature change is logged with timestamps, user attribution, and version snapshots. This audit trail supports FDA 21 CFR Part 11 and EMA Annex 11 inspection readiness.

Prescribe Professional Email Standards

Ensure every pharmaceutical email meets regulatory requirements and projects your brand with precision. Try Siggly free.