Sterovance Biotech – Dublin Market (Ireland)

“Quality Hormone APIs, Delivered to Dublin.”

Sterovance Biotech, a specialized pharmaceutical division of Zoesoe Exports Private Limited, is dedicated to the sourcing, marketing, and export of high-quality steroid and hormone Active Pharmaceutical Ingredients (APIs) to the Dublin pharmaceutical market in Ireland.

With a strong understanding of Ireland’s highly regulated pharmaceutical sector and regulatory framework under the Health Products Regulatory Authority, along with European oversight by the European Medicines Agency, Sterovance Biotech delivers APIs that meet stringent pharmacopeial standards such as Ph.Eur, USP, BP, and IP, ensuring compliance with Irish and EU requirements.

We cater to pharmaceutical manufacturers, contract manufacturing organizations (CMOs), biotech firms, formulation companies, importers, distributors, and research organizations in Dublin and surrounding regions, supporting regulated product development and compliant supply chains.

Our Presence in Dublin

Sterovance Biotech actively supports pharmaceutical and healthcare supply across Dublin, Cork, Galway, Limerick, and surrounding industrial zones.

Dublin is one of Europe’s leading pharmaceutical and biotech hubs, hosting major multinational pharmaceutical companies, advanced manufacturing facilities, and R&D centers. Ireland’s strong regulatory environment and export-oriented pharmaceutical industry make Dublin a strategic gateway for EU and global markets. We understand EU import procedures, documentation requirements, and regulatory expectations, enabling smooth and efficient API supply.

Manufacturing & Supply Advantage

All APIs are sourced from GMP-compliant manufacturing facilities in India, ensuring:

• Consistent quality and batch traceability

• Competitive pricing advantage for EU markets

• Reliable and continuous supply chain

• Compliance with HPRA, EMA, and international GMP standards

Sterovance Biotech operates through strategically aligned manufacturing locations, ensuring supply stability and regulatory consistency.

Regulatory & Documentation Support (Dublin / EU-Focused)

We provide complete documentation aligned with EU and Ireland import and registration requirements:

• COA (Certificate of Analysis)

• MSDS (Material Safety Data Sheet)

• DMF (ASMF – Active Substance Master File)

• CEP (Certificate of Suitability – EDQM)

• Stability Data (ICH Guidelines)

• GMP Certificates (EU-compliant)

• Export Documentation (Invoice, Packing List, COO, etc.)

• Support for EMA / HPRA regulatory requirements

Our Product Portfolio

Testosterone & Esters

Testosterone — USP/BP/IP/Ph.Eur | Testosterone Propionate — USP/BP/IP/Ph.Eur | Testosterone Enanthate — USP/BP/Ph.Eur | Testosterone Cypionate — USP | Testosterone Undecanoate — Ph.Eur/IH | Testosterone Decanoate — BP/IH

Nandrolone

Nandrolone (Base) | Nandrolone Decanoate — USP/BP/Ph.Eur/IP | Nandrolone Phenylpropionate — IH/IP

Boldenone

Boldenone — IH | Boldenone Undecylenate — IH

Methenolone

Methenolone Acetate — IH | Methenolone Enanthate — IH

Oxandrolone

Oxandrolone — USP/IH

Estrogens & Esters

Estradiol — USP/BP/IP/Ph.Eur | Estradiol Valerate — USP/BP/Ph.Eur | Estradiol Cypionate — USP | Ethinyl Estradiol — USP/BP/IP/Ph.Eur

Progesterone & Derivatives

Progesterone — USP/BP/IP/Ph.Eur | Hydroxyprogesterone Caproate — USP/IP/IH | Medroxyprogesterone Acetate — USP/IP | Dydrogesterone — USP/IP/BP/Ph.Eur | Norethisterone — BP/IP/Ph.Eur

Thyroid Hormone

Levothyroxine Sodium — USP/BP/IP/Ph.Eur

Insulin APIs (Biological Hormones)

Insulin Human (Recombinant) — USP/BP/IP/Ph.Eur

Our Working Process (Dublin Orders)

1. Send Inquiry
   API Name | Required Quantity | Dublin / Ireland / EU Requirement

2. Quotation & Pricing
   Competitive pricing | Availability | Delivery timeline

3. Order Confirmation
   Proforma Invoice | Order confirmation | Stock/Production allocation

4. Order Processing
   GMP manufacturing | Quality assurance | Batch traceability

5. Shipping & Logistics
   Air Freight (via Dublin Airport)
   Sea Freight (via Irish ports and EU distribution network)

6. Delivery
   Export-compliant packaging | Labeling as per EU norms | Tracking support

7. Documentation & Support
   COA | MSDS | ASMF | CEP | GMP | Export documents | EU regulatory support

Why Choose Sterovance Biotech for Dublin

• Competitive pricing tailored for EU pharmaceutical hub

• Strong experience with HPRA and EMA compliance

• GMP-certified sourcing from India

• Strategic logistics for EU and global distribution

• Availability of complete EU regulatory documentation (CEP, ASMF)

• Customized packaging and labeling as per EU regulations

• Complete regulatory and dossier support

• Transparent and ethical business practices

Your Trusted API Partner in Dublin

Sterovance Biotech is committed to supporting pharmaceutical companies and biotech firms in Dublin and across Ireland and Europe by delivering high-quality steroid and hormone APIs with full regulatory support and a reliable global supply chain.

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