YOU SEARCHED BY...
SEARCH BY...
Country
- Canada(4)
- Denmark(1)
- Germany(2)
- India(4)
- Italia (1)
- South Korea(1)
- United Kingdom(3)
- United States(47)
Company Spotlight
Recro
Quotient Sciences
Contract Service Directory
Kemwell Biopharma
Company Headquarters
511 Davis Drive
Suite 100
Morrisville, NC 27560
United States
Contract Service Directory
- 505(b)(2)
- Accelerated Stability Studies
- Aerosol Filling
- Analytical Laboratory Services
- Analytical Methods Development
- Analytical Validation Studies
- Animal Health
- Aseptic Processing
- Assay Development
- Biological Testing
- Biologics Manufacturing
- Biologics Process Development
- Bioprocess Validation
- Bioprocessing
- Bioprocessing, Disposable/Single-Use
- Biosimilars
- Blending
- Cell Culture Media Development
- Chiral Separations, R&D
- Chromatographic Analysis, LC/GC
- Chromatography
- Clean in Place / Sterilization in Place (CIP/SIP)
- Clinical Analysis
- Clinical Supply Management
- Clinical Trials, Phase III
- CMC (Chemistry, Manfacturing & Controls)
- Coating & Lamination
- Comparator Drug Blinding
- Comparator Drug Purchasing
- Contract Development and Manufacturing Organization (CDMO)
- Contract Manufacturing
- Contract Packaging
- Contract Research
- Dosage Form Development
- Downstream Processing
- Drug Development Services
- Encapsulation
- European QP
- Fermentation
- Filling, Capsule
- Filling, Syringe
- Filling, Vial
- Fluid Bed Processing
- Forced Degradation Studies
- Formulation Development
- Formulation Services
- Formulation, Controlled Release
- Granulation
- HPLC
- In Vitro Testing
- IND/NDA Submissions
- Lot Release Testing
- Lyophilization
- Mammalian Cell Culture
- Manufacturing, Aseptic Fill/Finish
- Manufacturing, Bioequivalence
- Manufacturing, Biologics
- Manufacturing, Capsules
- Manufacturing, Clinical Trials Supply
- Manufacturing, Controlled Substances
- Manufacturing, Creams & Ointments
- Manufacturing, Dose Form, Non-Sterile
- Manufacturing, Dose Form, Sterile
- Manufacturing, Ethical
- Manufacturing, Gels
- Manufacturing, Generics
- Manufacturing, Injectables
- Manufacturing, Liquids
- Manufacturing, Lyophilized Products
- Manufacturing, Oral Drug Delivery
- Manufacturing, Orally Dispersible Tablet
- Manufacturing, OTC
- Manufacturing, Other
- Manufacturing, Parenterals, Small Volume
- Manufacturing, Peptides
- Manufacturing, Powders, Non-Sterile
- Manufacturing, Powders, Sterile
- Manufacturing, Proteins
- Manufacturing, Semisolids
- Manufacturing, Solid Dosage
- Manufacturing, Solutions & Suspensions
- Manufacturing, Suppositories
- Manufacturing, Sustained Release
- Manufacturing, Syringes, Pre-filled
- Manufacturing, Tablets
- Manufacturing, Topicals
- Mass Spectrometry
- Methods Development
- Methods Validation
- Micro FT-IR Analysis
- Microbiological Testing
- Mixing & Blending
- Mixing and Granulating Equipment
- Packaging, Blister
- Packaging, Blister, Cold Form
- Packaging, Capsules
- Packaging, Clinical Trial Materials
- Packaging, Clinical Trials
- Packaging, Creams & Ointments
- Packaging, Injectables
- Packaging, Liquids
- Packaging, OTC
- Packaging, Parenterals
- Packaging, Solid Dosage
- Parenterals Development
- Parenterals, Syringe Filling
- Parenterals, Vial Filling
- Particle Characterization
- Particle Size Analysis
- Photostability
- Pilot-Scale Filling
- Polymerase Chain Reaction
- Preformulation
- Process Characterization
- Process Development/Scale-Up Services
- Process R&D
- Process Validation Studies
- Project Management
- Protein Extraction/Purification
- Protein Synthesis
- Purification
- QA/QC
- Quality Control Testing
- R&D Services
- Raw Materials Analysis
- Scale-Up
- Serialization
- Spray Drying
- Stability Studies
- Stability, ICH
- Sterile Filling
- Sterility Testing
- Sterilization
- Storage
- Syringe Filling
- Tablet Coating
- Technology Transfer
- Transdermals/Transmucosals
- UV-VIS Spectrophotometer Analysis
- Validation, Equipment Cleaning
- Validation, Filtration
- Validation, Manufacturing
Contract Services Directory
Content From Kemwell Biopharma
-
Selecting a Dosage Form for Drug Delivery to the Lungs
When initiating a development program for drug delivery to the lungs, selection of the dosage form warrants careful consideration.White Papers / Tech Papers Released on 05.19.2014
Related Content
-
Breaking News | Clinical Trial Materials | Collaborations & Alliances | Industry News | Preclinical Outsourcing
Ocugen Engages Kemwell Biopharma for cGMP Manufacture of OCU200
Paves the way towards getting OCU200 in the clinic by first half of 2022.Contract Pharma Staff 10.06.20
-
Biologics, Proteins, Vaccines
Will Immunotherapy Knock Out Cancer?
Innovative immunotherapy companies discuss with WuXi AppTec what’s next for this rapidly developing field ahead of BIO 2017.06.14.17
-
Breaking News | cGMP Manufacture | Clinical Trial Materials | Excipients | Facilities | Industry News
Lubrizol Unveils $60M Expansion Plan
Will invest in Particle Sciences, Vesta and other facilities in 201706.07.17
-
Breaking News | Promotions & Moves
-
Biosimilars
Indian Generic Firms Expand Biosimilar Portfolios
With more players entering the ring, the race to enter the promising biosimilars market is getting hotter by the day in IndiaS. Harachand, Contributing Editor 05.09.17
-
The Results Are In!
The growing need for analytical testing and clinical trials services are driving outsourcing demand.Tim Wright, Editor 05.09.17
-
Breaking News | cGMP Manufacture | Formulation Development | Industry News | Solid Dosage/Creams/Ointments
Catalent Manufactures Lexicon’s Xermelo Following Approval
To provide commercial supply of first-in-class oral therapy from its Kansas City facility05.09.17
-
Drug Development | Drug Discovery | Preclinical Outsourcing
Overcoming Preclinical Drug Development Hurdles
Aidan Synnott of Charles River Laboratories discusses the latest developments in oncology research modelsKristin Brooks, Contract Pharma 05.02.17
-
Analytical Services
Quality Risk Management
It’s not just for the big guys anymoreEmil W. Ciurczak, DoraMaxx Consulting 04.03.17
-
APIs | Cold Chain Management | Facilities | Serialization
-
Capsules | Solid Dosage/Semi-solids
Generic Drug Trends
Industry faces tighter capacity, consolidation, and drug pricing uncertaintyEdward S. Price, President, PCI 03.07.17
-
Solid Dosage/Semi-solids
Oral Solid Dosage Outsourcing: Trends & Challenges
Despite the increasing number of biologics, oral solids remain the dominant dosage form in the pharmaceutical market.Tim Wright, Editor, Contract Pharma 03.07.17
-
The Good, the Bad, and the Donald
Orphan drugs, CMO continuous manufacturing and developing world sales offer biggest revenue opportunities01.31.17
-
APIs | cGMP Manufacture
Navigating the Shifting Landscape of Contract API Manufacturing
What does it take for a CMO to succeed and grow in the current competitive marketplace?Saharsh Davuluri, Joint Managing Director, Neuland Labs 01.26.17
