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

Are You Keeping Pace With Oligo Synthesis Optimization?

From Readiness To Results: Unlocking Capacity For Expanding Product Demand

Advancing Topical Formulations With Innovative Preclinical Models

Accelerate Your pDNA And mRNA Process Development

Driving Robust Tech Transfer In Biologics: CFD Simulation

Practical Solutions For Protein Analytics And Residual DNA Testing

Choosing The Right Sporicide: Critical Factors For Robust Cleanroom Contamination Control

Driving Sustainability In Bioprocessing With Biobased Single-Use Solutions

Achieve Pharma 4.0 With Next Generation Software-Defined Manufacturing

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

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

The Successful Implementation Of A New Aseptic Filling Line

Determining And Controlling Oxygen Levels In Sensitive Formulations

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

Ensure Speed And Success With Your Drug Delivery Project

A Data-Driven Approach To Container Closure Integrity

Alba® Syringe Platform: Ensuring Stability For Sensitive Drugs

EU Med Device Regulations: Ensuring Compliance For Integral Combination Products

Selecting Container Closure Components: Extractables And Leachables

Using Positive Controls In Container Closure Integrity Studies

CCI Testing And Revisions To EU Annex 1

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

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

Advancing Precision And Automation In Injectable Drug Delivery

Visual Inspection Equipment To Deliver The Highest Product Integrity

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

Ensure Speed And Success With Your Drug Delivery Project

Alba® Syringe Platform: Ensuring Stability For Sensitive Drugs

Selecting Container Closure Components: Extractables And Leachables

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

The Journey Of A CDMO Choosing Pre-Sterilized Drug Containers

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

Nanoparticle Enabled Formulation And Drug Delivery Solutions

Water Activity Is A Critical Parameter For Microbial Stability

Patient- And Planet-Centric Bioavailability And Sustained Delivery

Formulation Of Crystalline Nanoparticles Enabling Superior Drug Load

Solvent-Free, Fusion-Based Amorphic Dispersion Process

Improve The Performance Of Your Small And Large Molecule Medicines

Oral Solid Dosage Products: Water Activity And Primary Packaging Selection

The Fusion-Based, Solvent-Free Process Disrupting Spray Drying

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

Improve The Bioavailability Of Poorly Soluble Drugs

Scaling Up A Revolutionary Amorphous Solid Dispersion Platform

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

Determining And Controlling Oxygen Levels In Sensitive Formulations

Using Positive Controls In Container Closure Integrity Studies

CCI Testing And Revisions To EU Annex 1

CESS Technology

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

Thermo Fisher Scientific EMEA Single-Use Technologies Capacity Expansion

Break Free From The Protein A Low-Productivity Paradigm

How To Maintain A Nuclease Free Environment During mRNA Production

How To Choose A Capping Method In MRNA Production

Scaling Up: Increasing Production Capacity While Reducing Costs

Singapore Single-Use Site Capacity Expansion

A Conceptual Overview Of The BioSMB MCC Platform

Solving The Analytics Bottleneck In Cell Line Development

Faciliflex Cleanroom Module For Therapeutic Drug Manufacturing

Your Contract Manufacturer Partner

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

Impact Of Water Activity On OSD Product Potency, Purity, And Bioavailability

Your Contract Manufacturer Partner

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

CentriPAK BioProcess Container Instructional Video

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

Ensure Speed And Success With Your Drug Delivery Project

Oral Solid Dosage Products: Water Activity And Primary Packaging Selection

Selecting Container Closure Systems With Confidence: Lyophilization

Determining CCI During Deep Cold Storage

CentriPAK BioProcess Container For Cell Culture Separations

The Enhanced Version Of Ready-To-Use Vial Platform

Protecting Oxygen Sensitive Formulations Throughout Product Life Cycle

Container Closure Integrity Of Product Requiring Deep Cold Storage

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

A Rapid Approach For Moisture Determination Of Lyophilized Product

A Practical Road Map For Compliance To EU GMP Annex 1

Why Add Water Activity To The Stability Test Protocol

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

Selecting Container Closure Systems With Confidence: Lyophilization

A Data-Driven Approach To Container Closure Integrity

Replacing Total Moisture Measurements By Water Activity Determination

The Container Closure Integrity Requirements In The Revised EU Annex 1

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

Supporting The Global Biopharma Industry With Single-Use Capacity Expansion

Singapore Single-Use Site Capacity Expansion

Robust And Consistent Frozen Storage And Shipment

Keep It Cool: Cellular Cryopreservation For Clinical Applications

The Way Forward: Supply Chain Solutions

Highly Flexible And Customizable On-Body Delivery System Platform

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

Thermo Fisher Scientific Single-Use Global Manufacturing Network

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

A Rapid Approach For Moisture Determination Of Lyophilized Product

The Pathway To Operational Readiness

Determining And Controlling Oxygen Levels In Sensitive Formulations

Compressed Gas Risk Assessment: A Significant Step In Your CCS

Revolutionizing Contract Manufacturing With A Unified QMS And MES Platform

Overcome The Hidden Complexities Of mRNA Process Development

Using Positive Controls In Container Closure Integrity Studies

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

CCI Testing And Revisions To EU Annex 1

Navigating GxP Compliance Challenges

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

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

Rapid Microbial Detection System For Earlier Results

Bioburden And EU GMP Annex 1: Risk Assessment, Reduction, And Testing

Workflow For Rapid Sterility Testing

The Future Of Robotics And Automation In QC In Microbial Testing Labs

The Route To Faster Microbial Quality Control

Expanding Capabilities In QC Analyses With Advanced LC Detection

An Efficient And Reliable Way To Digitalize Your Sterility And QC Testing Data

Determining And Controlling Oxygen Levels In Sensitive Formulations

Compressed Gas Risk Assessment: A Significant Step In Your CCS

Determining CCI During Deep Cold Storage

How To Optimize Labeling In A Pharmaceutical Environment

Impact Of Water Activity On OSD Product Potency, Purity, And Bioavailability

Faciliflex Cleanroom Module For Therapeutic Drug Manufacturing

Your Contract Manufacturer Partner

Bioburden And EU GMP Annex 1: Risk Assessment, Reduction, And Testing

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

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

The Impact Of Water Activity Testing On Tablets And Capsules

A Practical Road Map For Compliance To EU GMP Annex 1

An Efficient And Reliable Way To Digitalize Your Sterility And QC Testing Data

The Pathway To Operational Readiness

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

Attracting The Right Capital — Forming Partnerships For Long-Term Success

Deliver Contamination Control Solutions To An AUSTAR Customer

Water Activity Is A Critical Parameter For Microbial Stability

Faciliflex Cleanroom Module For Therapeutic Drug Manufacturing

AES Clean Technology Career Opportunities

Considerations & Steps For Building A Contamination Control Strategy (CCS)

Reduce Production Waste In Pharmaceutical Manufacturing

The Successful Implementation Of A New Aseptic Filling Line

ISO EN 17141 And ISO 14698 Overview

Viable Monitoring Solutions: Prepare Your Contamination Control Strategy (CCS) For EU GMP ANNEX 1

Customizable Solutions For Cleanroom Facility Monitoring

Single-Use Active Air Microbial Monitor Guidance

A Real-Time Viable Particle Counter To Identify Contamination Source

Driving Innovation In Decentralized Manufacturing

Cleanroom Partnership Showcase: Avid Bioservices

The Future Of mRNA Manufacturing

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

Best Practices For Cleanroom Project Delivery And Construction

Modular Cleanroom Panel Manufacturing Factory Tour

How mRNA Manufacturers Disrupt The Industry

AES Compass™ Cleanroom Facility Programming Video

Modular Facilities - The Proven Response For Rapid Biomanufacturing Anywhere

Cleanroom Conceptual Design Paradigm: Converting Spaces For GMP Operations

Cleanroom Design Cost Control

The Evolution Of Pharmaceutical Modular Cleanroom Technologies And Project Execution