PSUR Central – Costa Rica

PSUR Preparation & Review Services

Ministry of Health Costa Rica | DRPIS | US FDA | EU | WHO | PIC/S Aligned

PSUR Central is a specialized scientific arm of Zoesoe Exports Pvt Ltd, providing end-to-end Periodic Safety Update Report (PSUR) Preparation and Review Services for Costa Rica–based pharmaceutical manufacturers, Marketing Authorization Holders (MAHs), and authorized local representatives/importers supplying to the Costa Rican market and regulated international destinations.

Since 2008, PSUR Central has supported pharmaceutical companies globally with regulatory-compliant, authority-acceptable PSUR documentation, enabling smooth compliance with the Ministry of Health of Costa Rica, uninterrupted product renewals, and effective post-marketing safety management.

Who We Support in Costa Rica

PSUR Central works closely with:

• Costa Rican pharmaceutical manufacturers and MAHs
• Authorized local representatives and licensed importers
• Companies importing products from US, EU, India, LATAM & other regulated markets
• Firms managing post-marketing safety obligations under Costa Rican regulations
• Regulatory Affairs (RA) and Pharmacovigilance (PV) teams
• Companies preparing PSURs for registrations, renewals, variations, and routine submissions

Our services are designed to meet Costa Rica regulatory expectations while fully aligning with international pharmacovigilance requirements.

Our PSUR Services – Costa Rica

We provide complete lifecycle support for PSUR documentation, including:

• PSUR preparation as per Costa Rica Ministry of Health / DRPIS requirements
• PSURs aligned with US FDA, EU, WHO, PIC/S & exporting country MOHs
• Independent technical and regulatory review of existing PSURs
• Support for health authority queries post-submission
• Safety data gap assessment against current global PV guidelines
• Customization of PSURs based on product type, approval status, and source markets
• Supply of authority-acceptable, ready-to-use PSUR templates

All PSURs are science-driven, non-generic, and authority-ready.

Regulatory Standards Followed

Our PSUR documentation is prepared in alignment with:

• ICH E2C (R2) Guidelines
• WHO Pharmacovigilance Guidelines
• EU GVP Module VII
• US FDA post-marketing safety requirements
• PIC/S-aligned regulatory frameworks
• Costa Rica Ministry of Health pharmacovigilance requirements
• Country-specific formats and reporting timelines

Product Types & Therapeutic Coverage

• Prescription pharmaceutical products
• Over-the-counter (OTC) medicines
• Fixed-Dose Combinations (FDCs)
• APIs (where applicable)
• Herbal and traditional medicines (subject to Ministry of Health acceptance)

Why Companies in Costa Rica Choose PSUR Central

• Regulatory-focused, globally acceptable PSURs
• Templates accepted across Central America, LATAM & international markets
• Strong expertise in Latin American health authority interactions
• Robust safety data evaluation and signal detection
• Reduced regulatory observations and follow-ups
• Confidential, professional, deadline-driven execution
• Deep understanding of Costa Rica’s import-driven pharmaceutical market

How We Support You

To initiate PSUR preparation or review, we typically require:

• Product registration and approval details
• Approved labeling (PI / SmPC)
• Sales and patient exposure data
• Adverse event summaries
• Costa Rica submission timelines

Based on this information, our team provides a customized technical scope, timelines, and commercial proposal aligned with Costa Rica Ministry of Health and global regulatory requirements.

PSUR Central

Global PSUR Compliance. Science-Driven. Authority-Ready.
Supporting pharmaceutical companies, MAHs, and authorized representatives in Costa Rica with globally acceptable pharmacovigilance documentation.

If you’d like, I can also:
✔ Add Costa Rica–specific PSUR FAQs
✔ Create a concise Spanish–English landing page
✔ Convert this into a brochure or regulatory PDF
✔ Localize further for Central America / LATAM multi-country strategies