Sidefarma

Sidefarma

Sidefarma is a CMO specialized in the manufacture of small and medium size batches for pharmaceutical companies across the world in regulated markets following European quality.

About the plant

SIDEFARMA is a CMO based in Portugal, specialized in the manufacture of differentiated and customized size batches of solid (coated tablets, tablets, capsules and powder sachets), semi-solid (creams, ointments, gels and suppositories) and liquid (syrups and solutions) dosage forms. Always accompanying the progress and trends of the Pharmaceutical Industry, SIDEFARMA relies on more than 45 years of technological experience and is continuously reinforcing its production capacities.

We are specialized in the manufacturing of small to medium scale batches.

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Certifications

• ISO
• EMA (EU GMP)
• UAE Ministry of Health & Prevention

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Activity

• Oral liquids and semisolids, Oral solids / OSD, Topical, mucosal and transdermal, Bottles, Tubes, Sprays, Oral solutions, Oral suspensions, Oral emulsions, Syrups, Oral gels, Tablets, Hard capsules, Granules / Pellets, Powders, Semisolid forms, Liquid forms, FDF / DRUG PRODUCTS manufacturing

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Features

• Uses: Commercial (Phase IV), Human
• Toxicity (OEB classification): 1 / low-hazard (PDE > 5,000 µg/day), 2 (PDE = 1,000 - 5,000 µg/day), 3 (PDE = 100 - 1,000 µg/day)
• DEA: N/A
• BSL: N/A
• Therapeutic areas: N/A
• Markets: DIGEMID (Peru), EMA (EU), PMDA (Japan), Health Canada (Canada), MHRA (UK), TGA (Australia), EDE (UAE), SFDA (Saudi Arabia), Turkish Health Authorities

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Batch Size / Reactor

• Small, Medium

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Services

• Manufacturing services, Analytical / QC services, Quality Assurance services, Packaging, Tech transfer, Pilot plant, Formulation mixing, Engineering batches, Scale-up, Pilot batches, Registration batches, Batch records, Analytical methods development, Analytical methods validation, Analytical methods transfer, QP in house, Batch certification / release, GMP documentation, Primary packaging, Secondary packaging, Labeling, Serialization

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