- AgRay experts have over 20 years experience working with CMOs to complete your formulation process from intermediate to full API.
- We have the expertise to implement manufacturing processes from early stage to intermediate and final finished product.
- A complete end to end support can be provided from lab to registeration.
CLINICAL & QUALITY MANAGEMENT
- On site and off site GMP mock audit based on EU standards
- Clinical trial designs & project managemnt
- Scientific advice and health authority meetings
- Medical writing and literature search
- Bio-equevalent studies
REGULATORY To MaRKET
- eCTD data dossier coversion
- Dossier GAP analysis
- Full dossier writting
- User readability testing of PIL
- Regulatory strategy advisory
- Market authorisation submission
- Lifecycle maintenance
- Regulatory attairs project outsourcing
Talk to Us
API & Finished dosage licensing brokerage
Most pharmaceutical company have their in house business development experts in charge of overseeing product in and out licensing. We are able to step in and bridge the gap between drug manufacturers and major distributors.
Licensor can be sure of their product license sales for quick recouperation of investment in product development without affecting your long term strategic market sales.
Lincensee will be provided variety of viable products based on their local maket demand.
- We know where your products are needed.
- We advice our partners on the viability of your products in their respective markets.
Business development & emerging market access
AgRay have partnered with on the ground companies in different geographical regions to provide unmatched penetration into market that are still alien to European and Asian based pharmaceutical companies.
Just ask our experts for market analysis and demand areas based on therapeutic indications that are primary target of your pharmaceutical and derma products.
- We understand the market
- We know the market demand strength
- We have established contacts to tap into, at a moment notice.