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Top Features
Seven Core Pieces of the Puzzle: What to Consider When Selecting an Analytical Lab
Bridging the Divide: Understanding Contrasting Approaches in Drug Development
Updates on the Value of a Day of Delay in Drug Development
CEO Spotlight: Matthew Stober
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FDA Approves Roche's Itovebi for Breast Cancer
Evonik to Restructure Keto and Pharma Amino Acid Business
Hubble Therapeutics Selects Andelyn to Manufacture Clinical Grade AAV
Cellipont Bioservices, Mongoose Bio Partner to Advance MGB-001
Lipocine Enters Exclusive Supply and Distribution Agreement with Pharmalink
APIs
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Cytotoxics and High Potency Manufacturing
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Solid Dosage/ Creams/ Ointments
Evonik to Restructure Keto and Pharma Amino Acid Business
Application of QbD Approach for Tech Transfer and Process Characterization of Biologics
Rommelag CDMO
Hubble Therapeutics Selects Andelyn to Manufacture Clinical Grade AAV
Cellipont Bioservices, Mongoose Bio Partner to Advance MGB-001
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Solid Dosage / Semi-solids
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Nipro Launches D2F Glass Vials Using Stevanato's EZ-fill Technology
Thermo Fisher Scientific to Leverage DHL Express GoGreen Plus Service
SK pharmteco, Cryoport Partner for Cell and Gene Therapy Logistics and BioServices
Pharma Matters Q&A: Rising Above the Rest
Avara Highlights Recent Expansions and Core Capabilities
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Application of QbD Approach for Tech Transfer and Process Characterization of Biologics
Hubble Therapeutics Selects Andelyn to Manufacture Clinical Grade AAV
Arbele Enters AI Alliances in Precision Oncology and Manufacturing
Panthera Biopartners Joins Parexel Site Alliance Vaccine Network
Lilly, insitro Enter Strategic Agreements for Metabolic Diseases
Filtration & Purification
GMPs/GCPs
Inspections
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Regulatory Affairs
Validation
Rottendorf Pharma Selects ValGenesis VLMS
FDA sIRB Mandate: A Chance to Reassess Site Performance
Rottendorf Pharma Selects ValGenesis’ VLMS
U.S. House of Representatives Passes the BIOSECURE Act
Post-COVID Trends in Biopharma Contract Manufacturing
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APIs
Aseptic Processing
cGMP Manufacture
Cleaning Validation
Clinical Trial Materials
Cytotoxics and High Potency Manufacturing
Excipients
Extractables and Leachables
Facilities
Fill/Finish
Lyophilization
Parenterals
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Solid Dosage/Creams/Ointments
Risk Management
Mitigating Risk in Your Hardware and Single-Use Products Selection Process
Key things to understand on your journey to a successful selection process.
Online Exclusives
Carrie Lloyd, Account Executive
08.26.24
cGMP Manufacture
|
Drug Development
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Risk Management
Manufacturing Agreements in the Cell & Gene Therapy Space
Tips to avoid IP contamination in manufacturing agreements such as using limits on liability/liability caps and confidentiality.
April Wurster, Partner, Snell & Wilmer
06.14.24
Industry News
|
Risk Management
Examining the Role of AI in Supply Chain Management Across the Bio/Pharma Industry
Key findings from DCAT Research & Benchmarking’s survey on the emerging role of AI in supply chain management.
Online Exclusives
Charles Sternberg, Associate Editor
05.15.24
Parenterals
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Risk Management
Drug Shortages Threaten Patients: How Pharma Can Build Supply Chain Resilience
Preventing drug shortages with supply chain risk assessment.
Online Exclusives
Charles Sternberg, Associate Editor
04.19.24
Breaking News
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Industry News
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Risk Management
Ginkgo Acquires Key Assets of Reverie Labs
Strengthens its AI/ML-driven discovery services offering and accelerates its work to build next-gen biological foundation models.
02.28.24
APIs
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Breaking News
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Collaborations & Alliances
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Excipients
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Industry News
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QA/QC
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Risk Management
Valisure, DoD Conduct Pharmaceutical Quality Risk Assessment Study
Partnership will generate objective drug quality data through independent sourcing and testing.
08.14.23
APIs
|
Drug Development
|
Risk Management
How Respiratory Protection Upgrades Safeguard Pharma Manufacturing
The use of PAPRs and SARs is increasing due to potential drug potency exposures during manufacturing and greater awareness of respiratory technology advances.
Biologics, Proteins, Vaccines
|
Clinical Trials
|
Drug Development
|
Inspections
|
Process Validation
|
Risk Management
Establishing Commercial Manufacturing Services for Antibody-Drug Conjugates
Learn how to properly structure your development work, perform a thorough process risk assessment and prepare for pre-approval inspection audit.
Sponsored
released by
Merck
06.09.21
APIs
|
Drug Development
|
Risk Management
Small-Molecule Drug Development: Advantages of an Integrated, Phase-Based Approach
Small-molecule drug development has become more complex and challenging, leading to greater reliance on CDMOs.
Sarah Bethune, Cambrex
09.09.20
Analytical Services
|
Breaking News
|
Risk Management
CluePoints Tech Benefits Clinical Studies Affected by COVID-19
Its COVID-19 risk assessment package and Data Surveillance solution is being utilized in over 200 ongoing studies.
Contact Pharma Staff
05.07.20
Bio News
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cGMP Manufacture
|
Industry News
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Regulatory Affairs
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Risk Management
Stellar Announces Positive Third-Party Trial Results
The company's KLH manufacturing methods have achieved robust viral clearance
05.29.18
Bio News
|
cGMP Manufacture
|
Drug Delivery
|
Facilities
|
Industry News
|
Laboratory Testing
|
Risk Management
Quay Expands Specialist Isolation Suites
The suites are to support the development of potent drugs in a protective environment
03.06.18
Breaking News
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cGMP Manufacture
|
Drug Delivery
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Industry News
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Risk Management
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Supply Chain
Pharmapack 2018 Announces Winners
The six winners were chosen across two categories: Exhibitor Innovation and Health Product
Videos
Breaking News
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Industry News
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QA/QC
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Risk Management
Sanofi to Transform its Contracting Foundation
Selects Icertis’ digital platform for cloud management
09.01.17
Drug Development
|
Risk Management
Mitigating Regulatory Risk for a Global Product Launch
Addressing the critical regulatory challenges life science companies face in today's market
Online Exclusives
Kristin Brooks, Contract Pharma
11.22.16
APIs
|
Clinical Trials
|
Drug Development
|
Information Technology
|
Regulatory Affairs
|
Risk Management
News Highlights from the 2016 Annual DIA Meeting
Comprehend Launches Clinical Intelligence Suite, Quintiles Launches CGM Service Offering, and more...
Online Exclusives
07.06.16
Drug Development
|
Excipients
|
Lyophilization
|
Risk Management
Clinical Manufacturing On Time and Within Budget
...
David Brett, Vetter Pharma International GmbH
06.02.16
Biosimilars
|
Risk Management
India Revises Biosimilars Guidelines
Stricter quality, safety norms on cards
S. Harachand, Contributing Editor
05.05.16
APIs
|
Cleaning Validation
|
Clinical Trials
|
Drug Development
|
Drug Discovery
|
Risk Management
|
Toxicology
|
Validation
Setting Health-Based Exposure Limits to Support Pharmaceutical Development and Manufacturing
Health-based exposure limits are needed to support risk assessments
B.D. Naumann, P.J. Nigro, U. Bruen, L. Parola, D. Cragin and A. Schatz, Merck & Co., Inc. and Ashland, Inc.
05.05.16
Drug Delivery
|
Drug Development
|
Excipients
|
Process Development
|
Process Validation
|
Risk Management
|
Validation
Process Development Trends
An approach to process development of pMDIs using cold fill and pressure fill technology
Steve Haswell, 3M Drug Delivery Systems
05.05.16
Breaking News
FDA Approves Roche's Itovebi for Breast Cancer
Evonik to Restructure Keto and Pharma Amino Acid Business
Hubble Therapeutics Selects Andelyn to Manufacture Clinical Grade AAV
Cellipont Bioservices, Mongoose Bio Partner to Advance MGB-001
Lipocine Enters Exclusive Supply and Distribution Agreement with Pharmalink
View Breaking News >
CURRENT ISSUE
September 2024
Seven Core Pieces of the Puzzle: What to Consider When Selecting an Analytical Lab
Bridging the Divide: Understanding Contrasting Approaches in Drug Development
Updates on the Value of a Day of Delay in Drug Development
CEO Spotlight: Matthew Stober
CDMO Specialization
Post-COVID Trends in Biopharma Contract Manufacturing
Pharma’s Next Frontier: GLP-1s and Other New Therapies
CEO Spotlight: Prasad Raje
HPAPIs Soar Riding the Targeted Drugs Wave
View More >