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Looking for a GMP approved CMO for Manufacturing and Packaging of CBD Transdermal Patches [ENA09497]
A fully integrated European based medical cannabis company is looking for a GMP approve CMO for Manufacturing and Packaging of Cannabidiol transdermal patches. The packaging should be single patches in packs of 5. The required quantity is MOQ. The final market is Europe.
14 Jan 2021

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Looking for a CMO for Re-Packaging Oncology Injectable Products in the United States [ENA09492]
An international pharmaceutical company that focuses on the commercialization of therapies is looking for a CMO for Re-Packaging Oncology Injectable Products.
14 Jan 2021

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Looking for a USFDA and MHRA certified CMO to Manufacture Oncology Tablets [ENA09485]
A multinational company that primarily develops medicines to treat respiratory, cardiovascular disease, arthritis, diabetes, weight control and depression is looking for a USFDA and MHRA certified CMO having spray drying & solvent handling capability for Oncology Tablets. The required quantity is 1,500,000 units to 2,000,000 units. The packaging will be in bottle and blister pack. The project launch timing is Q3 2027. The final market is EU and the US.
13 Jan 2021

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Looking for a CDMO for Manufacturing of Eye Drops [ENA09473]
An independent consultant is looking for a CDMO for the Manufacturing of Eye Drops in the packaging of 10 ml. The required quantity is 50,000 units. The project launch timing is March/April 2021. Interested suppliers can contact them via their email: tidyfella47@yahoo.com.
12 Jan 2021

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Looking for a USFDA certified CMO to Manufacture NSAID Oral Suspension [ENA09464]
One of the leading global pharmaceutical company having a strong presence in the regulated markets is looking for a USFDA certified CMO for Manufacturing of NSAID Oral Suspension. The packaging will be in a bottle. The project launch timing is 2022. Following are the required dosage strengths:
1. 0.5 mg/ ml in 15 ml Oral Suspension. The required quantity is 5,921 units.
2. 0.5 mg/ ml in 30 ml Oral Suspension. The required quantity is 961 units.
3. 1.5 mg/ ml in 10 ml Oral Suspension. The required quantity is 2,198 units.
4. 1.5 mg/ ml in 32 ml Oral Suspension. The required quantity is 4,397 units.
5. 1.5 mg/ ml in 100 ml Oral Suspension. The required quantity is 5,602 units.
6. 1.5 mg/ ml in 180 ml Oral Suspension. The required quantity is 4,116 units.
11 Jan 2021

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Looking for a USFDA/ FDA/ SFDA/ EFDA approved CMO to Manufacture Black Seed Softgels [ENA09258]
An Independent consultant is looking for a USFDA/ FDA/ SFDA/ EFDA approved CMO to Manufacture Black Seed Softgels (cold-pressed). The required quantity is 1,500 bottles (60 units/ bottle). Interested service provider can contact them via their email: emadaabdul@gmail.com.
10 Dec 2020

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Looking for a USFDA/ TGA/ APVMA approved Analytical Service Provider [ENA09256]
A manufacturing company that produces quality veterinary products is looking for USFDA/ TGA/ APVMA approved Analytical Service Provider for In-Vitro Dissolution Testing of Metronidazole Paste (BCS Class- I Drug) formulation (vet) to support the efficacy and safety. The packaging type and size is 30 g and 60 g syringe.
10 Dec 2020

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Looking for a GMP approved CMO to Manufacture Sterile product intended for Intravenous Applications [ENA09251]
A company that focuses on biomolecular research and development in regenerative therapies is looking for GMP approved CMO to Manufacture Sterile products (parenteral) intended for intravenous applications for lipid metabolism or cognitive functions. The required quantity is 1,000 - 2,000 units in the first year and 2,000 - 4,000 units in the coming years. The packaging will be in Bottles (25 ml and 50 ml). The project currently is in the preclinical phase. The launch time of the project is 2021.
09 Dec 2020

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Looking for a GMP & USFDA approved CMO to Manufacture Parsley Glycerin Soft Gel Capsules [ENA09244]
A neutraceutical startup firm is looking for a GMP and USFDA approved CMO to Supply and Manufacture Parsley Glycerin Soft Gel Capsules from that meniscus for CD 38 inhibitor compound. The required quantity is 500,000 units to 1,000,000 units in the first year. Packaging will be in bottles (30 units or 60 units/ bottle). The country of distribution is 70% USA, 20% Europe, 10% rest of the world.
09 Dec 2020

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Looking for a USFDA & GMP approved CMO for Sublingual Delivery [ENA09208]
A company that deals in the drug development projects is looking for a USFDA & GMP approved CMO for Sublingual Delivery for a Phase 1 CTM for rare disease but chronic indication. The dosage form is oral, considering liquid solution/suspension or capsule as well but at the moment looking for Sublingual delivery. IND scheduled for Q4 2021 so manufacturing and testing to be completed prior to November 1, 2021. For a phase 1 trial, hundreds of doses only and probably two strengths. The country of distribution is initially US and then Canada, Europe and Japan later.
03 Dec 2020

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