News
All News
Publications
All PublicationsPharmTechPharmTech Europe
Multimedia
All VideosAsk the ExpertBehind The HeadlinesDrug Digest VideosDrug Solutions Podcast
Conferences
Conference CoverageConference Listing
More
Webcasts
Resources
ICH Q9 Revision: A Comprehensive Resource on Quality Risk ManagementPartnersPeer-Reviewed ResearchPharmTech ProductsPharma InsightsSponsored PodcastsSponsored VideosSponsored eBooksState of the ScienceWhitepapers

Subscribe

  • News
  • Publications
  • Multimedia
  • Conferences
  • Webcasts
  • Resources
  • Subscribe
  • Analytics
    • Bio/Pharmaceutical Analysis Techniques
    • Laboratory Equipment and Instruments
  • Data and Artificial Intelligence
  • Dosage Forms
    • Solid/Semi-Solid Dosage
    • Specialty Dosage Drugs
    • Parenterals and Injectables
    • Inhalation Drugs
  • Drug Development
    • Intellectual Property and Patents
    • Process and Scaling
    • APIs and Excipients
    • Ingredients
    • Formulation and Drug Delivery
  • Manufacturing
    • Aseptic/Sterile Processing
    • Equipment
    • Process and Automation
    • Manufacturing, Parenterals and Injectables
    • Manufacturing, Biosimilars and Biobetters
    • Manufacturing, Inhalation Drugs
    • Manufacturing, Solid and Semi-Solid Dosage Drugs
    • Manufacturing, Cell Therapies
    • Manufacturing, Biologic Drugs
    • Supply Chain
    • Manufacturing, Gene Therapies
    • Packaging and Distribution
  • Outsourcing
    • Contract Research Services
    • Contract Analytical Services
    • Contract Development Services
    • Regulatory Consulting
    • Logistics and Distribution
    • Contract Manufacturing Services
  • Quality Systems
    • Ask the Expert
    • Quality Assurance/Quality Control
    • Regulatory Oversight and Compliance
Spotlight -
Analytics|
Dosage Forms|
Drug Development|
Manufacturing|
Outsourcing|
Quality Systems
Advertisement
News|Articles|May 18, 2016

Best Practices for Product Transfer

Author(s)Sponsor's Content
Advertisement

Newsletter

Get the essential updates shaping the future of pharma manufacturing and compliance—subscribe today to Pharmaceutical Technology and never miss a breakthrough.

Subscribe Now!
Advertisement

Related Content

Advertisement

Why Pharma’s AI Agents Need Smaller, Domain-Specific Models First

ByJayaprakash Nair
December 3rd 2025
Hand holding a stylus over a tablet with futuristic risk management icons such as warning signs, data charts, and safety symbols on a dark background. | Image Credit: ©ImageFlow -stock.adobe.com

How a “Plan, Prevent, Prove” Approach Helps Avoid Facility and Equipment Problems

BySusan Haigney
December 2nd 2025

FAQ: Everything to Know about 3D Printing in Pharma Manufacturing and Packaging

ByPatrick Lavery
November 30th 2025
Comparator Selection & Supply: Best Practices for Clinical Success

Comparator Selection & Supply: Best Practices for Clinical Success

ByCatalent
November 20th 2025
CNPV Survey

Share Your Perspective on the Commissioner’s National Priority Vouchers Program

ByChristopher Cole
November 14th 2025
Advertisement
Advertisement

Trending on Pharmaceutical Technology

1

Batch Certification for New Manufacturing Technologies: The Qualified Person Role in a Digital Environment

2

Why Pharma’s AI Agents Need Smaller, Domain-Specific Models First

3

Drug Digest: Closing the Gap in Modern Process Control and Automation for QC/QA

4

How a “Plan, Prevent, Prove” Approach Helps Avoid Facility and Equipment Problems

5

BirchBioMed’s Idiopathic Pulmonary Fibrosis Treatment Receives Orphan Drug Designation

  • About Us
  • Advertise
  • Contact Us
  • Editorial Info
  • Editorial Advisory Board
  • Do Not Sell My Personal Information
  • Privacy Policy
  • Terms and Conditions
Contact Info

259 Prospect Plains Rd, Bldg H
Cranbury, NJ 08512

609-716-7777

Brand Logo

© 2025 MJH Life Sciences®

All rights reserved.

Home
About Us
News
Contact Us