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Implementing an Automated DOE in Twin Screw Wet Granulation
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The Centralized Data Collection Platform Revolutionizing Credible Tracking in Pharma
...
Steve Beda, Executive Vice President, Trax Technologies
03.11.24
Facilities
Pharma Engineers Discuss Sustainability Challenges & Solutions
A new survey shows how leading life sciences firms are embedding sustainability strategy into facility engineering and CAPEX programs.
Aisling Crowley, Head of Client Relations, Unispace Life Sciences
02.01.24
Clinical Trials
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Cold Chain Management
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Logistics
|
Supply Chain
Clinical Trials: Trends & Insights
Ensuring success in the dynamic and evolving EU clinical trials landscape.
Leandro Moreira, Senior Vice President of Corporate Development, Yourway
11.14.23
Unleashing Superpower Potential
How space is the key ingredient.
Katie Nelson & Mairi Dillon, Kadans Science Partners
10.12.23
Beyond the Pill
The pharmaceutical industry has evolved from a drug developer to a solution provider.
Natalia de la Figuera, Co-founder and COO, Genesis Biomed
09.13.23
QA/QC
PUPSIT!
What is it? Should I? Must I? How do I? Where do I?
Carmine Stropoli, PE, Life Sciences Technologist
07.19.23
Drug Development
|
Information Technology
Embracing Automation to Support Drug Development
Finding the right method and level of automation to support pharmacovigilance needs and increase efficiency.
Mike Gordon, CEO, ArisGlobal
05.03.23
3 Important Questions to Ask Before Starting a Clinical Pharmacology Program
Developing a robust strategy early in your clinical program can save time and resources.
Amanda Mathis, Director of Clinical Pharmacology, Rho
04.04.23
Big Pharma Expands R&D Base in India
Offshoring to support drug development.
S. Harachand, Contributing Editor, Contract Pharma
03.10.23
Supply Chain
Beat the Supply Chain Backlog
How accelerated project timelines are key to meeting demand in the pharmaceutical industry.
Dave Mitchell, Global Director of Life Science Products, JBT’s A&B Process
02.06.23
Information Technology
The Role of Artificial Intelligence in Drug Discovery
...
Haydn Boehm, Director of Product Marketing, Dotmatics
11.07.22
QA/QC
|
Regulatory Affairs
Automation Is Key to Meeting Demands in Pharmacovigilance
To handle the spike in safety reports and improve general efficiencies with adverse event reporting, the industry is turning to newer technologies.
Bruce Palsulich, Vice President of Product Strategy, Oracle Health Sciences
10.03.22
Keeping Quality Levels High in your CMO Relationships
Building a comprehensive quality and compliance strategy when partnering with CMOs is vital for success.
Bill Connell, Principal, Supply Chain Practice Leader, Tunnell Consulting
09.07.22
CDMOs Face Ukraine Heat
Manufacturers realign their supply chains to lessen the impact.
S Harachand, Contributing Writer
07.11.22
QA/QC
|
Regulatory Affairs
Be Safer by Doing Less: The Future of Zero Touch AE Case Processing
AI & NLP Technology are critical to overcoming current adverse event processing challenges.
Updesh Dosanjh, Practice Leader, Pharmacovigilance Technology Solutions, IQVIA
06.07.22
Information Technology
|
QA/QC
5 Key Characteristics of a Next Generation QMS Solution
Pharmaceutical companies must modernize their QMS to provide equal or greater value in today’s world of digital tools and information.
Kari Miller, QMS Regulatory and Product Management Leader, Global Tech Solutions, IQVIA
04.04.22
Drug Discovery
Indian Drug Makers Ramp Up Discovery Research
CDMOs augment capabilities.
S. Harachand, Contributing Writer
03.08.22
Regulatory Affairs
Improving Public Health
Regulatory considerations around bioequivalence in topical generic drug product development.
John Buchan, Life Science Technology Specialist
02.01.22
Solid Dosage/Creams/Ointments
Bioequivalence in Topical Generics
Regulatory considerations around bioequivalence in topical generic drug product development.
Charles Evans, Marc Brown and Jon Lenn, MedPharm
11.09.21
QA/QC
Three Tips for Navigating Post-Approval Pharmacovigilance
Seamlessly transition from regulatory reporting to post-approval safety surveillance in today’s market.
Emmanuel Belabe, ArisGlobal and Nina Patel Lahanis, Eversana
10.06.21
Breaking News
Parexel Announces CEO Transition
DifGen Acquires FDA-Registered Manufacturing Facility
Quotient Sciences Makes Executive Leadership Team Appointments
Plenaries Discuss AI and Next-Gen Modality Development at AAPS NBC
SCHOTT Pharma Invests $371M in U.S. Prefillable Syringe Mfg. Facility
View Breaking News >
CURRENT ISSUE
March 2024
Implementing an Automated DOE in Twin Screw Wet Granulation
Sustainable Pharmaceutical Packaging
Pre-filled Syringe Packaging Trends
Liquid Pharmaceutical Filling: Small, Smaller, Micro Batches
Newsmakers Q&A: BioVectra
Multi-particulate Formulations – Tablets or Capsules?
Manufacturing Equipment Trends
OSD Outsourcing: Savvy CMOs Hone Skills as Complex APIs Fuel Demand
Catalent Acquisition by Novo Holdings: Evolution of the Industry(?)
The Road Ahead for CDMOs in 2024
View More >