NDA and product feasibility review
We sign a confidentiality agreement and review your product brief, target market, and existing documentation.
Private-label manufacturing managed from Singapore, produced at our GMP manufacturing partner, registered with HSA, and distributed in Singapore.
INNORINI PTE. LTD. (UEN 202015523Z) provides pharmaceutical OEM and private-label manufacturing, managed from Singapore and produced at our qualified GMP manufacturing partners. We handle formulation, production, HSA registration, Singapore-based unit-dose packing, and distribution in Singapore. Minimum order quantities depend on dosage form and packaging and are confirmed at the feasibility stage.
At a glance
Pharmaceutical OEM (Original Equipment Manufacturing) in Singapore involves a Singapore-registered company contracting a licensed manufacturer to produce medicines or health supplements under the client's brand name. The Singapore company acts as the commercial and regulatory lead, managing product registration, import, quality control, and distribution, while manufacturing takes place at a GMP-certified facility.
Innorini's model combines cost-effective GMP manufacturing capacity through our partners with Singapore's rigorous regulatory framework and trusted market access. This gives overseas brands the best of both: competitive production costs and the credibility of a Singapore-registered, HSA-compliant supply chain.
| Company | INNORINI PTE. LTD. |
|---|---|
| UEN | 202015523Z |
| Singapore Address | 1 Clementi Loop, #05-02 Clementi West LogisPark, Singapore 129808 |
| Manufacturing Partner | Qualified GMP partner network |
| Singapore Divisions | Innorini services, Lyrus Life Sciences, Innorini Stabicon |
| Regulatory Capability | HSA registration, SAR, variations, renewals, post-market |
| Local Operations | Licensed wholesale, import coordination, unit-dose packing |
| Markets | Singapore; other markets by arrangement |
| Dosage Forms | Tablets, capsules, powders, liquids, topicals |
| B2B Contact | sales@innorini.com.sg |
Through our qualified GMP manufacturing partners, we support a range of dosage forms including:
Specific capabilities, minimum order quantities, and lead times depend on the product type, formulation complexity, and packaging requirements. We provide a detailed feasibility assessment after reviewing your product brief.
| Capability | Available | Where Performed | Notes |
|---|---|---|---|
| Product formulation | Yes | Partner network / Singapore | Via our GMP manufacturing partners R&D |
| Technology transfer | Yes | Partner network | From client or existing formula |
| GMP manufacturing | Yes | GMP partners | Qualified GMP partner sites |
| Stability studies | Yes | Partner facilities | ICH-compliant protocols |
| HSA dossier preparation | Yes | Singapore | Full CTD format support |
| Import & customs clearance | Yes | Singapore | Import permits and customs clearance coordinated to HSA requirements |
| Unit-dose packing | Yes | Clementi, Singapore | Dedicated unit-dose system |
| Wholesale distribution | Yes | Singapore | HSA Therapeutic Products Wholesaler’s Licence (on the public HSA register) |
Through our GMP manufacturing partner network and our Singapore regulatory team, we support products across a wide range of therapeutic categories. Our experience spans both prescription and consumer healthcare products.
Laxatives, antacids, proton pump inhibitors, ORS and electrolyte products, anti-diarrhoeals.
Paracetamol, NSAIDs, topical analgesics, combination cold and flu formulations.
Antihistamines, decongestants, cough preparations, throat sprays and antiseptics.
Topical creams, ointments, antiseptics, skincare and barrier repair formulations.
Antihypertensives, lipid-lowering agents, anti-diabetics, cardiovascular generics.
Vitamins, minerals, herbal supplements, sports nutrition, hangover and wellness products.
Antibiotics, antifungals, topical antiseptics, povidone-iodine formulations.
Pet care products, animal health supplements, topical treatments for companion animals.
Iron supplements, prenatal vitamins, hormonal preparations, feminine care products.
We sign a confidentiality agreement and review your product brief, target market, and existing documentation.
We determine the correct HSA classification (therapeutic product, health supplement, or exempt) and the appropriate registration pathway.
our GMP partner network finalises the formulation, analytical specifications, and a formal quality agreement between all parties.
GMP production through our qualified partners with full batch records, certificates of analysis, and stability data.
We prepare and submit the regulatory dossier to HSA, managing all queries and requests for additional information.
Upon HSA approval, we finalise import licensing, product labelling, and artwork compliance.
Products are shipped to Singapore, cleared through customs, and undergo incoming quality inspection at our Clementi facility.
We handle storage, optional unit-dose packing, wholesale distribution, and ongoing post-market compliance and pharmacovigilance.
These terms are often used interchangeably but have distinct meanings:
Innorini offers all three models depending on your product stage and requirements. Visit our CDMO Singapore page for development-focused services.