Market Reports

Industry leaders join the 2021 Cleanroom Conference

Leading industry names to join the virtual and in-person event taking place in September 2021.

Pre-travel cleanroom quarantine for a trip to Mars: Building an isolator

Comecer talks through the ISO Class 3 isolator they were commissioned to help with for building ExoMars, a mission that plans to send a lander to release a rover on the surface of Mars in 2020

Interview with Mark Kendrick | Stancold

The great variety in industries that can be worked on with cleanrooms, is a draw for many to work in the specialism. Senior Business Development Manager for Stancold, Mark Kendrick, explains how the recently launched cleanroom division at the company came to be and how his team and the sector are continuing to respond and adapt

Jumping on the vaccine trend: Designing the facility

If vaccines weren’t an increasing market before 2020, they most definitely are now. Designing a vaccine-specific facility solution that is not only quick to market but can stand the test of time is more important than ever explains David Lindholm from KeyPlants

US market report | A year full of problems, 365 days of solutions

Times are changing as the pandemic affects manufacturing at every level. US cleanroom suppliers are the thermometer to these changes, seeing the effects first as they have to meet increasing domestic demand in crisis conditions. Speaking to Claire Barber from PBSC, Bret Asper from Clean Rooms International, and Charles Lipeles from Mecart sheds light on the situation as it is today

Interview with Jessica Rayser | Charles River Laboratories

Microbial monitoring is key to a well functioning cleanroom. Project Manager for Charles River's Accugenix services, Jessica Rayser, goes into depth about sustainability in EM procedures, the pandemic, and the future of rapid microbial methods

Pharmaceutical reshoring: a healthy requirement, a strategic necessity

More than a year into the COVID-19 crisis, the novel coronavirus continues to disrupt our societies, including how the pharmaceutical industry operates; Andrew Badrot, CEO of C<sup>2</sup> PHARMA, discusses the ongoing ramifications of the pandemic

Back to basics: Control your zones

The sanitation process varies depending on the industry, but Patricia Sitek from CR Konsulting talks about common ways to categorise areas in a facility from any sector, and some golden rules to follow for them

How do flexible film isolators shape up?

The ‘flexibility’ of flexible film isolators represent a real benefit in today’s rapidly evolving pharmaceutical landscape. Validating their use for APIs and HPAPIs means demonstrating that they can go toe to toe with rigid designs for operator protection. Written by Martyn Ryder

Assessing disinfection rotation at the point of use: Designing a field trial

Qualifications required for disinfectants consist of three phases: suspension tests, surface tests and field trials. The first two phases are well-described as either European or US standards, with surface testing against a range of representative surfaces being regarded as providing a more robust challenge than the suspension test. What is not described in any standard is the field trial. Written by Tim Sandle

Interview with Shawn Manuel | AirCare Automation

Connecting the technical and business sides of a company, Global VP of Sales for AirCare Automation, Shawn Manuel, discusses his view on the cleanroom controls sector

Interview with Stephen Pygott | Biopharma Group

Matching the customer to the product they need requires in depth knowledge of the wider concept of application. Airflow product specialist, Stephen Pygott, is one such expert whose laboratory centric background gives him an interesting and unique take on the safety cabinet market

The importance of growth promotion testing

Given the critical nature of microbiological quality tests which are employed to ensure that pharmaceutical products are safe for human use, it is in turn essential to undertake quality control (QC) tests to ensure that the culture media being used for these is fit for purpose and performs properly. Cherwell Laboratories' Steven Brimble explains

Virucidal testing of cleanroom disinfectants

In “normal” times, with the exception of live vaccine manufacturers, control of viruses in cleanrooms is not usually the highest priority within contamination control. Viruses need a host to survive, as they are obligate parasites, just nucleic acid surrounded by a protein that can only replicate within a host cell, so their ability to survive on hard, dry surfaces is minimal. Contec’s Neil Simpson explains

The details of dust extraction in controlled environments

To choose the right machine, the nature of the dust and the statutory regulations for its handling and removal, as well as classification of the machine and filter technology, must be considered. Daniel Took from archer reminds us, the lower the Threshold Limit Value (TLV) for dust, the higher the health risk

A to Z of an effective monitoring programme

A successful monitoring process allows control of contamination for regulatory or product yield reasons. John Merrill from C2C explains monitoring results can be used for trend analysis by comparing data with subsequent air samples, and alert and action levels can be set for results outside of set acceptable thresholds

Clothing solution for EU GMP Annex I

Only single-use cleanroom apparel will help sterile product manufacturers improve compliance with the new guidelines, as Franck Bureth of Kimberly-Clark Professional explains

Jo Nelissen | ABN Clean Technology

In an interview, the founder and CEO of Belgium-based cleanroom engineering company discusses the issues of 2020 and his opinion on the growing cleanroom practices and technologies of today

Speaking opportunities for Cleanroom experts

Industry experts from the cleanroom industry are invited to submit their presentations for the Cleanroom Technology Conference in July

Germany market report | Supporting the vaccine race

A country that is taking on many fronts of the pandemic response, Germany has a well-known pharmaceutical landscape and an enviable cleanroom backbone. But is it enough?

Should technology based ARMMs be more widely adopted?

New technologies now exist that can reduce the time taken to detect viable particles by almost comical percentages, while also detecting and distinguishing inert ones. Therefore, it is puzzling why the uptake of ARMM devices in aseptic pharma manufacturing seems so slow

Validating VPHP bio-decontamination of FFP masks

DeconBox is a Vapour-Phase-Hydrogen-Peroxide bio-decontamination system that allows FFP2 and FFP3 masks to be reused. Riccardo Volta and Giacomo Nicolini from Comecer explain the process of validating the mobile, purpose-built system for use in controlled settings

Manipulators: A gamechanger in radiopharmaceutical production

For many years manipulator technology has stagnated, but recently, remotely controlled manipulator design has shown a leap forward. Jim Peterson from Central Research Labs discusses the variety of these machineries that help keep operators and radioactive material separate

Martin Birch and Peter Makowenskyj| G-CON Manufacturing

The modular construction movement is an unstoppable train at this point. In an exclusive interview, two G-CON Directors discuss the trajectory of this expanding technology, and how multiple global crises are changing business on both sides of the pond

Trending Articles

  1. Combustible dust in pharma: An elusive but very real risk Controlling contamination and controlling hazards simultaneously in today's cleanrooms is difficult, sometimes even oppositional. Many operations have serious gaps that are difficult to reconcile without the proper expertise. J.T. Cochran from CRB Group discusses
  2. The importance of growth promotion testing Given the critical nature of microbiological quality tests which are employed to ensure that pharmaceutical products are safe for human use, it is in turn essential to undertake quality control (QC) tests to ensure that the culture media being used for these is fit for purpose and performs properly. Cherwell Laboratories' Steven Brimble explains
  3. How-to guide: Pass box qualification Material transfer equipment plays an important role in minimising contamination risks during the manufacturing process. Industry expert, Jesus Casas, gives an overview of available pass boxes and a step-by-step explanation on how to qualify them appropriately
  4. Cleanroom tightness and room pressurisation: Discrepancy? A cascaded room-pressure regime has been considered for decades to prevent cross-contamination of different processes. But Harald Flechl from ISPE says today's tight cleanrooms must have leaks to ensure a room-pressure regulation - so why should we build tight cleanrooms?
  5. HVAC cleanroom design calculation explained Mecart's Charles Lipeles dissects the key considerations to factor in the drawing board

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CPhI Worldwide

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