Douglas Cdmo | Third Party Audit | PharmaCompass.com

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Douglas CDMO

VIRTUAL BOOTH, Contact Details

DIGITAL CONTENT

2 Corporate Content #SupplierSpotlight, 3 Data Compilation #PharmaFlow, 34 News #PharmaBuzz

DEVELOPMENTS

7 Drugs in Development

7 Drugs in Development

FINISHED DOSAGE FORMULATIONS

41 FDF Dossiers, 1 FDA Orange Book, 40 Listed Dossiers

SERVICES

Packaging, Drug Product Manufacturing, API & Drug Product Development

Packaging
- 1 Contract Services
- 4 Clinical Services
Drug Product Manufacturing
API & Drug Product Development
- 10 Formulation Development

KEY SERVICES

Tablet Contract Manufacturing, Modified Release Tablet Manufacturing, Capsule Contract Manufacturing, Chewable Tablet Manufacturing, Highly Potent Drug Product Manufacturing, CDMO for Softgel Capsules, Clinical Manufacturing of Tablets, Clinical Supply of Capsules, Coated Tablet Manufacturing, CDMO for Modified Release Formulations, CDMO for Capsule Manufacturing

INSPECTIONS & REGISTRATIONS

7 FDA, 1 GDUFA, 2 Third-Party Audit

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AuditGMP Pharma

Get Site Audit

AuditGMP Pharma SL delivers ISO 17020-accredited GMP audits and compliance services with expert, reliable, and tailored solutions.

Douglas Manufacturing Ltd.

Country : New Zealand

City/Region : Lincoln

Audit Date : Aug-23

Audit Type : On-Site

02

AuditGMP Pharma

Get Site Audit

AuditGMP Pharma SL delivers ISO 17020-accredited GMP audits and compliance services with expert, reliable, and tailored solutions.

Douglas Manufacturing Ltd.

Country : New Zealand

City/Region : Lincoln

Audit Date : Apr-26

Audit Type : On-Site

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Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.