Drug Product
Analytical & Bioanalytical Services
Company Overview
About
SIDEFARMA is a pharmaceutical CDMO offering comprehensive services.
Key Expertise
Specialized in API Manufacturing, Sterile Fill/Finish, Lyophilization
Therapeutic Areas
Cardiovascular
Endocrinology
Quick Facts
HQ:Portugal
Founded:2015
Employees:1,818
Capabilities & Services
Core Capabilities
- Sterile Injectable
- Sterile Fill/Finish
- Fill/Finish (Vials)
Types of Organization
GMP Manufacturing
Quality Systems
Regulatory Support
Dosage Forms
Cartridge / Pen
Containment Capabilities
OEB 5 (≤1 µg/m³)
Cytotoxic / ADC Handling
Production Scales
Pilot Scale
Phase I Clinical Trials
Clinical
Markets Served
Asia-Pacific
Regulatory Approvals
Drug Approval HWGH33
Health Canada · #APR-UQPBZSSL · 2018-11-01
Certifications
FDA Registration
U.S. Food and Drug Administration
Cert #: CERT-KAF2LN8K
Issued: 2020-03-24
Expires: 2025-08-26
WHO GMP
World Health Organization
Cert #: CERT-JKZ9X4AB
Issued: 2020-06-22
Expires: 2025-10-26
MHRA GMP
UK Medicines and Healthcare products Regulatory Agency
Cert #: CERT-5C3CEQWH
Issued: 2020-08-15
Expires: 2025-09-06
Health Canada GMP
Health Canada
Cert #: CERT-AYE7BAEZ
Issued: 2020-04-23
Expires: 2025-06-28
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Key facts about SIDEFARMA
- SIDEFARMA is headquartered in Portugal.
- SIDEFARMA was founded in 2015.
- SIDEFARMA has 1,818 employees.
- SIDEFARMA's capabilities include Sterile Injectable, Sterile Fill/Finish and Fill/Finish (Vials).
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