Peruvian Clinical Trial Authorization Form

Streamline Your Clinical Trial Authorization Process in Peru

Conducting clinical trials in Peru requires navigating complex regulatory frameworks involving the Instituto Nacional de Salud (INS), ethics committee approvals, and strict participant data protection protocols. This Peruvian Clinical Trial Authorization Form provides pharmaceutical companies, research institutions, and clinical research organizations with a comprehensive, compliant solution for submitting trial applications.

Built for Peruvian Regulatory Compliance

This template addresses the specific requirements mandated by SUNAT, INS, and Peruvian health authorities. It captures essential sponsor information including RUC numbers, principal investigator credentials, detailed study protocols, ethics committee certifications, and comprehensive participant data protection plans aligned with Peruvian Law No. 29733 (Personal Data Protection Law).

Whether you're a multinational pharmaceutical company, university research department, or clinical research organization operating in Peru, this form ensures you collect all necessary documentation and declarations required for regulatory submission.

Integrate with Your Research Workflow

Paperform's powerful integration capabilities mean your clinical trial applications can flow directly into your project management systems, CRM platforms, or document repositories. Send notifications to legal teams, sync with Airtable or Google Sheets for tracking, and use Stepper to automate multi-stage approval workflows—routing applications to different review committees, triggering follow-up tasks, and maintaining audit trails without manual intervention.

For forms requiring formal signatures from principal investigators, ethics committee chairs, or institutional representatives, integrate Papersign to convert submissions into legally binding documents with secure eSignatures, keeping your entire authorization process digital and compliant.

Professional, Secure, and SOC 2 Compliant

Clinical trial data demands the highest security standards. Paperform is SOC 2 Type II certified and offers data residency controls, ensuring your sensitive research protocols, participant information, and proprietary study data remain protected. With role-based permissions, you can control which team members access specific sections of submitted applications.

Trusted by research organizations worldwide, this template helps you maintain compliance with Peruvian regulations while presenting a professional, organized application to INS and ethics committees—accelerating your approval timeline and getting your critical research started faster.