Gabriela Mikhaiel, marketing manager at Dec Group explains how a fully integrated isolator and process equipment solution offers high safety, efficient control and cleaning features as well as full compliance in terms of manufacturing regulations.
Karen Rossington from Contec discusses how a new good manufacturing practice regulation is set to impact cleaning programmes within the pharmaceutical industry.
Michael Avraam, head of solutions engineering at ChargePoint Technology explains how containment valves and wireless monitoring mitigate risk during HPAPI manufacture.
Here, Karen Rossington and Siobhan Murphy from Contec guide readers through the implications of the EU Biocidal Products Regulation (BPR) on life science cleanroom users.
John Rush subject matter expert — HVAC, from specialist cleanroom design and construction provider BES, discusses strategies for designing more energy efficient cleanrooms.
Michael Avraam, global product manager at ChargePoint Technology discusses the evolution of containment strategies, specifically within the role of containment verification and monitoring technology.
Howorth Air Technology and Russell Finex reveal how combining their expertise allowed them to create multiple customised solutions for a new production facility.
Dujuan Lu, PhD (technical client manager/global lead, SGS Life Science Services) and Kate Comstock (senior marketing specialist, Thermo Fisher Scientific) assess whether or not contaminants leach out from single-use bioprocess bags
Pharmaceutical companies are unwittingly putting production processes at risk of contamination by fitting mechanical seals which fail to comply with EU regulations. says John Smiddy, European Sales and Technical Support Director for AESSEAL.
Containment solutions for OSD are primarily concerned with the safety of those involved in producing life-saving medication — the operators. Marcus Behrens, vice president Sales Pharma Solid, Bosch Packaging Technology, goes into more detail…
