The CMC Regulatory Landscape During Product Development, Manufacturing

Solving The Inhalation Puzzle: A CDMO's Guide To Dry Powder Development

CRISPR Meets LNPs: A New Era In Cell And Gene Therapies

Scaling Up Your E. Coli pDNA Process From Parameter Screening To Pilot Scale

What Your Environmental Monitoring Isn't Telling You

The Pathway To Operational Readiness

Proven Strategies For GxP Compliance And Inspection Readiness

Cleanroom Conceptual Design Paradigm: Converting Spaces For GMP Operations Part 2

Unlocking Efficiency In Large-Scale Microbial Manufacturing

Seals And Stability: Preventing Failures In Synthesis And Chromatography Columns

Optimizing The Progression Of Biotherapeutic Candidates To FIH Studies

A New Look At Subcutaneous mAb Delivery Using Nanoformed Particles

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

Driving Excellence In Aseptic Fill-Finish: A Strategic Partnership With Stäubli Robotics

CCI Testing And Revisions To EU Annex 1

The Successful Implementation Of A New Aseptic Filling Line

Selecting Container Closure Components: Extractables And Leachables

Oxygen Permeation In Pre-Filled Syringes

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

New Guidelines For Container Closure Integrity Testing

Non-destructive Moisture Analysis Of Freeze Dried Product

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

Mycap® Bottle Closures – Aseptic Fluid Transfer Systems For Bottles

EU Med Device Regulations: Ensuring Compliance For Integral Combination Products

Reliable Visual Inspection Equipment To Deliver The Highest Product Integrity For Patient Safety

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

Selecting Container Closure Components: Extractables And Leachables

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

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

Ensure Speed And Success With Your Drug Delivery Project

Advancing Precision And Automation In Injectable Drug Delivery

Alba® Syringe Platform: Ensuring Stability For Sensitive Drugs

The Journey Of A CDMO Choosing Pre-Sterilized Drug Containers

Technology To Overcome Absorption Hurdles And Solubility Limitations

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

Scaling Up A Revolutionary Amorphous Solid Dispersion Platform

Oral Solid Dosage Products: Water Activity And Primary Packaging Selection

Patient- And Planet-Centric Bioavailability And Sustained Delivery

USP <922> Water Activity Testing For Oral Solid Dose Pharmaceuticals

Water Activity Is A Critical Parameter For Microbial Stability

Improve The Bioavailability Of Poorly Soluble Drugs

Improve The Performance Of Your Small And Large Molecule Medicines

Nanoparticle Enabled Formulation And Drug Delivery Solutions

Formulation Of Crystalline Nanoparticles Enabling Superior Drug Load

Solvent-Free, Fusion-Based Amorphic Dispersion Process

CCI Testing And Revisions To EU Annex 1

Non-destructive Moisture Analysis Of Freeze Dried Product

Determining And Controlling Oxygen Levels In Sensitive Formulations

Using Positive Controls In Container Closure Integrity Studies

Technology To Overcome Absorption Hurdles And Solubility Limitations

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

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

Single-Use Technology For Quality mRNA Manufacturing

Your Contract Manufacturer Partner

Redefine Your Oligonucleotide Manufacturing

Showcasing A Scalable Downstream Platform For Multiple AAV Serotypes

Solving The Analytics Bottleneck In Cell Line Development

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

Scaling Up A Revolutionary Amorphous Solid Dispersion Platform

Thermo Fisher Scientific Single-Use Global Manufacturing Network

Thermo Fisher Scientific Suzhou, China Manufacturing Site Capabilities

Your Contract Manufacturer Partner

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

Oral Solid Dosage Products: Water Activity And Primary Packaging Selection

Selecting Container Closure Systems With Confidence: Lyophilization

Selecting Container Closure Components: Extractables And Leachables

Managing Risks In Injectable Drug Delivery

How To Optimize Labeling In A Pharmaceutical Environment

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

New Guidelines For Container Closure Integrity Testing

Navigating Primary Packaging Challenges, Solutions For Emerging Innovators

CentriPAK BioProcess Container Instructional Video

Determining CCI During Deep Cold Storage

Why Add Water Activity To The Stability Test Protocol

USP <922> Water Activity Has Opened A Door For OSD Manufacturers

USP <922> Water Activity Testing For Oral Solid Dose Pharmaceuticals

Selecting Container Closure Systems With Confidence: Lyophilization

Replacing Total Moisture Measurements By Water Activity Determination

A Rapid Approach For Moisture Determination Of Lyophilized Product

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

A Practical Road Map For Compliance To EU GMP Annex 1

New Guidelines For Container Closure Integrity Testing

The Container Closure Integrity Requirements In The Revised EU Annex 1

Rapid Non-Destructive Product Moisture Determination In Stability Studies

Container Closure Integrity Of Product Requiring Deep Cold Storage

Thermo Fisher Scientific Single-Use Global Manufacturing Network

Supporting The Global Biopharma Industry With Single-Use Capacity Expansion

Keep It Cool: Cellular Cryopreservation For Clinical Applications

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

Highly Flexible And Customizable On-Body Delivery System Platform

Singapore Single-Use Site Capacity Expansion

The Way Forward: Supply Chain Solutions

Robust And Consistent Frozen Storage And Shipment

CCI Testing And Revisions To EU Annex 1

Oxygen Permeation In Pre-Filled Syringes

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

A Rapid Approach For Moisture Determination Of Lyophilized Product

The Pathway To Operational Readiness

Navigating GxP Compliance Challenges

Revolutionizing Contract Manufacturing With A Unified QMS And MES Platform

Compressed Gas Risk Assessment: A Significant Step In Your CCS

Non-destructive Moisture Analysis Of Freeze Dried Product

Overcome The Hidden Complexities Of mRNA Process Development

Determining And Controlling Oxygen Levels In Sensitive Formulations

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

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

Expanding Capabilities In QC Analyses With Advanced LC Detection

CCI Testing And Revisions To EU Annex 1

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

Selecting Container Closure Components: Extractables And Leachables

Data Integrity In The Quality Control Lab: No Pen, No Pain

Oxygen Permeation In Pre-Filled Syringes

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

The Route To Faster Microbial Quality Control

Workflow For Rapid Sterility Testing

Rapid Microbial Detection System For Earlier Results

How To Optimize Labeling In A Pharmaceutical Environment

Simplifying Bioprocess Data Collection

The Impact Of Water Activity Testing On Tablets And Capsules

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

Your Contract Manufacturer Partner

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

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

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

Selecting Container Closure Components: Extractables And Leachables

Navigating Special Regulatory Pathways For Advanced Therapy Development Success

Faciliflex Cleanroom Module For Therapeutic Drug Manufacturing

Managing Risks In Injectable Drug Delivery

A Practical Road Map For Compliance To EU GMP Annex 1

Scope 3 Emissions: Cut The Complexity With Creative Collaboration

AES Clean Technology Career Opportunities

USP<1788>2022 Revision Summary

Deliver Contamination Control Solutions To An AUSTAR Customer

Safety Department At Cleanroom Manufacturer Ensures No One Gets Hurt

Get Your Aseptic Facility Ready For EU GMP Annex 1

Particle Measuring Systems' FMS Solution At Argonaut Manufacturing Services

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

The Successful Implementation Of A New Aseptic Filling Line

Cleanroom Manufacturer Expands Capacity To Meet Industry Needs

Data Quality - The Journey Of The Data Management Life Cycle

Water Activity Is A Critical Parameter For Microbial Stability

AES Compass™ Cleanroom Facility Programming Video

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

Modular Assembly Equipment For Flexible And Scalable Solutions

Modular Cleanroom Panel Manufacturing Factory Tour

How To Best Optimize mRNA Production Workflows

Cleanroom Design Cost Control

Litebeam LED Cleanroom Lighting

The Evolution Of Pharmaceutical Modular Cleanroom Technologies And Project Execution

Standardizing Modular Cleanrooms For Faster-To-Market Drug Manufacturing

The Future Of mRNA Manufacturing

Cleanroom Conceptual Design Paradigm: Converting Spaces For GMP Operations

Best Practices For Cleanroom Project Delivery And Construction