Five Practical Considerations To Move From Concept To Clinic

Bridging The Gap Between Product Readiness And Equipment Availability

Automating Visual Inspection Qualification

When A Logbook Project Becomes A Digital Movement

Lessons From FDA 483s And Warning Letters: Cleanroom Compliance

Eliminate Risk From Your Viral Vector Tech Transfers

Navigating Regulatory Expectations For Injectable Packaging

Cleanroom Changes In 2026 For Better Contamination Control

Extrusion-Based ASD Scale-Up: Performance Through Process Understanding

Streamlining pDNA: Capacity, Complexity, And Cutting-Edge Solutions

EU GMP Annex 11: Compliance Strategy And Digital Solutions

Boost Quality For More Efficient Tablet Manufacturing

MG America Virtual Pharma Expo September 2025: Oral Solid Dose Manufacturing And Packaging

KORSCH Virtual Pharma Expo September 2025: Oral Solid Dose Manufacturing And Packaging

Syntegon Virtual Pharma Expo May 2025: Aseptic Manufacturing And Packaging

Pioneering Precision In Pharma And Radiopharma Solutions

Integrate Advanced Equipment Into Your Cleanroom Facilities

Step Into The Future Of ATMP Fill-Finish

Overview Of Biological Indicator And Sterilization Monitoring Systems

Does Blow/Fill/Seal Aseptic Packaging Make Sense for Your Drug?

AST Virtual Pharma Expo May 2024

A Data-Driven Approach To Container Closure Integrity

Alba® Syringe Platform: Ensuring Stability For Sensitive Drugs

CCI Testing And Revisions To EU Annex 1

The Successful Implementation Of A New Aseptic Filling Line

EU Med Device Regulations: Ensuring Compliance For Integral Combination Products

Mitigating Ultracold Storage And Transport Risk With CCIT

Ensure Speed And Success With Your Drug Delivery Project

Using Positive Controls In Container Closure Integrity Studies

Early-Stage Considerations For The Selection Of Pre-Fillable Syringes When Developing A Vaccine

Determining And Controlling Oxygen Levels In Sensitive Formulations

EZ-fill® Kit: RTU Packaging Solutions For Fast Access To Small Volumes

EZ-fill Smart™ Enhancing Aseptic Fill-Finish Efficiency In Pharmaceutical Manufacturing

Alba® Syringe Platform: Ensuring Stability For Sensitive Drugs

Advancing Precision And Automation In Injectable Drug Delivery

The Journey Of A CDMO Choosing Pre-Sterilized Drug Containers

UPLC Columns: Fundamentals, Chemistries, And Selected Small-Molecule Applications

Ensure Speed And Success With Your Drug Delivery Project

Visual Inspection Equipment To Deliver The Highest Product Integrity

EZ-fill® Kit: RTU Packaging Solutions For Fast Access To Small Volumes

EZ-fill Smart™ Enhancing Aseptic Fill-Finish Efficiency In Pharmaceutical Manufacturing

Selecting Container Closure Components: Extractables And Leachables

Improve The Bioavailability Of Poorly Soluble Drugs

Patient- And Planet-Centric Bioavailability And Sustained Delivery

Oral Solid Dosage Products: Water Activity And Primary Packaging Selection

Formulation Of Crystalline Nanoparticles Enabling Superior Drug Load

Improve The Performance Of Your Small And Large Molecule Medicines

Technology To Overcome Absorption Hurdles And Solubility Limitations

Scaling Up A Revolutionary Amorphous Solid Dispersion Platform

Future Of Pharma Packaging: Trends, Tech, And Patient Solutions

Water Activity Is A Critical Parameter For Microbial Stability

Nanoparticle Enabled Formulation And Drug Delivery Solutions

Solvent-Free, Fusion-Based Amorphic Dispersion Process

Improving Bioavailability, Drug Loads, And Pill Burdens Of Solid Dispersions

CCI Testing And Revisions To EU Annex 1

Future Of Pharma Packaging: Trends, Tech, And Patient Solutions

Using Positive Controls In Container Closure Integrity Studies

Determining And Controlling Oxygen Levels In Sensitive Formulations

Developing Modular Facility Proof-Of-Concept For Multi-Modal Bioprocessing

Improve The Bioavailability Of Poorly Soluble Drugs

Rapid Process Development And Technical Support For AAV Scaleup

A Conceptual Overview Of The BioSMB MCC Platform

How To Choose A Capping Method In MRNA Production

Thermo Fisher Scientific Suzhou, China Manufacturing Site Capabilities

Scaling Up: Increasing Production Capacity While Reducing Costs

Intensification Strategies For Upstream, Downstream Processes

The Route To Faster Microbial Quality Control

Improve The Performance Of Your Small And Large Molecule Medicines

Technology To Overcome Absorption Hurdles And Solubility Limitations

Solving The Analytics Bottleneck In Cell Line Development

Determining CCI During Deep Cold Storage

The Enhanced Version Of Ready-To-Use Vial Platform

Managing Risks In Injectable Drug Delivery

Oral Solid Dosage Products: Water Activity And Primary Packaging Selection

Key Considerations When Developing Your Combination Product

CentriPAK BioProcess Container Instructional Video

Alba® Syringe Platform: Ensuring Stability For Sensitive Drugs

Selecting Container Closure Systems With Confidence: Lyophilization

A Science-Based Approach For Ensuring Container Closure Integrity Of Sterile Vials

Future Of Pharma Packaging: Trends, Tech, And Patient Solutions

Ensure Speed And Success With Your Drug Delivery Project

Human Factors Testing: Engaging End-Users In Med Device Development

A Data-Driven Approach To Container Closure Integrity

The Container Closure Integrity Requirements In The Revised EU Annex 1

Replacing Total Moisture Measurements By Water Activity Determination

Survival Kit For Quality Regulations: A Closer Look At Lyo Packaging

Rapid Non-Destructive Product Moisture Determination In Stability Studies

Selecting Container Closure Systems With Confidence: Lyophilization

A Practical Road Map For Compliance To EU GMP Annex 1

Protecting Oxygen Sensitive Formulations Throughout Product Life Cycle

Mitigating Ultracold Storage And Transport Risk With CCIT

A Science-Based Approach For Ensuring Container Closure Integrity Of Sterile Vials

Container Closure Integrity Of Product Requiring Deep Cold Storage

Why Add Water Activity To The Stability Test Protocol

Supporting The Global Biopharma Industry With Single-Use Capacity Expansion

Robust And Consistent Frozen Storage And Shipment

Thermo Fisher Scientific Single-Use Global Manufacturing Network

Singapore Single-Use Site Capacity Expansion

Early-Stage Considerations For The Selection Of Pre-Fillable Syringes When Developing A Vaccine

Keep It Cool: Cellular Cryopreservation For Clinical Applications

The Way Forward: Supply Chain Solutions

Highly Flexible And Customizable On-Body Delivery System Platform

Overcome The Hidden Complexities Of mRNA Process Development

Navigating GxP Compliance Challenges

Compressed Gas Risk Assessment: A Significant Step In Your CCS

Airflow Visualization Studies: The Impact Of Annex 1 On Sterility Assurance

CCI Testing And Revisions To EU Annex 1

Using Positive Controls In Container Closure Integrity Studies

Determining And Controlling Oxygen Levels In Sensitive Formulations

The Pathway To Operational Readiness

Meet The Experts: Part 1 - Process Analytical Technology (PAT)

A Rapid Approach For Moisture Determination Of Lyophilized Product

Revolutionizing Contract Manufacturing With A Unified QMS And MES Platform

Determining CCI During Deep Cold Storage

Webinar On-Demand: Substitution Of Hazardous Substances

Compressed Gas Risk Assessment: A Significant Step In Your CCS

Microbial Sampling Of Compressed Gas Has Never Been So Simple And Safe

The Route To Faster Microbial Quality Control

CCI Testing And Revisions To EU Annex 1

Mitigating Ultracold Storage And Transport Risk With CCIT

Workflow For Rapid Sterility Testing

Maximizing Safety In The Daily Handling Of Hazardous Goods In The Lab

Rapid Microbial Detection System For Earlier Results

Using Positive Controls In Container Closure Integrity Studies

Determining And Controlling Oxygen Levels In Sensitive Formulations

How To Optimize Labeling In A Pharmaceutical Environment

Clinical Strategy For Successful Cell And Gene Therapy — How Did I Get Here?

A Data-Driven Approach To Container Closure Integrity

The Container Closure Integrity Requirements In The Revised EU Annex 1

Survival Kit For Quality Regulations: A Closer Look At Lyo Packaging

Managing Risks In Injectable Drug Delivery

Navigating GxP Compliance Challenges

Compressed Gas Risk Assessment: A Significant Step In Your CCS

Key Considerations When Developing Your Combination Product

A Practical Road Map For Compliance To EU GMP Annex 1

EU Med Device Regulations: Ensuring Compliance For Integral Combination Products

Importance Of Architectural Layout To Prevent Contamination

Faciliflex Cleanroom Module For Therapeutic Drug Manufacturing

Cleanroom Manufacturer Expands Capacity To Meet Industry Needs

A Real-Time Viable Particle Counter To Identify Contamination Source

Get Your Aseptic Facility Ready For EU GMP Annex 1

Annex 1 Ready Cleanroom Classification Testing

Compressed Gas Risk Assessment: A Significant Step In Your CCS

Airflow Visualization Studies: The Impact Of Annex 1 On Sterility Assurance

Data Quality - The Journey Of The Data Management Life Cycle

USP<1788>2022 Revision Summary

Real-Time Information On Microbial Contamination In Pharma Cleanrooms

The Successful Implementation Of A New Aseptic Filling Line

Deliver Contamination Control Solutions To An AUSTAR Customer

Particle Measuring Systems' FMS Solution At Argonaut Manufacturing Services

Biopharma Resilience: Bionova Scientific Talks Capacity, Speed, And Agility

The Future Of mRNA Manufacturing

The Evolution Of Pharmaceutical Modular Cleanroom Technologies And Project Execution

Addressing Rapid Biomanufacturing Capacity Needs

Modular Facilities - The Proven Response For Rapid Biomanufacturing Anywhere

Best Practices For Cleanroom Project Delivery And Construction

Importance Of Architectural Layout To Prevent Contamination

Time And Cost Savings Of Modular Cleanrooms Vs. Stick Built Cleanrooms

How mRNA Manufacturers Disrupt The Industry

Litebeam LED Cleanroom Lighting

Cleanroom Conceptual Design Paradigm: Converting Spaces For GMP Operations

Standardizing Modular Cleanrooms For Faster-To-Market Drug Manufacturing