There are many reasons why organisations need to document their SOPs. From ensuring uniformity in end products to training staff and meeting regulatory demands. Good SOPs are the key to quality assurance and sharing organisational knowledge efficiently. But how do you actually write them so they have maximum impact?What is...
XCAM Jointly Awarded Funding To Strengthen UK Space Sector Partnerships
UK based XCAM Ltd, world leaders in specialist digital camera systems, have jointly been awarded grant funding from the UK Space Agency (UKSA) via its International Bilateral Fund (IBF) - Phase 1. The funded project is being led by the Open University (OU) working with the Indian Space Research Organisation...
Two Key Appointments for Medilink Midlands
Life science industry organisation Medilink Midlands has announced the permanent appointment of Melanie Davidson as Chief Executive Officer, and Andrea Dawson as Chief Financial and Operating Officer. Having both fulfilled their roles in an interim capacity since March 2023, Melanie and Andrea are now permanently appointed to their new positions....
A spotlight on Medilinks Partner & Relationship Manager: Jo Bekis
Jo Bekis, joined the Medilink Midlands team in 2023, and brings with her a wealth of skills to support our membership community. Jo is prioritising time to meet with all of our Patrons and Members, to understand their business, any challenges they may be facing, and how best Medilink Midlands...
The Importance of GxP Auditing for Pharmaceutical Companies
As a pharmaceutical company, ensuring that your products are safe, effective, and compliant with regulatory requirements is essential. One way to achieve this is through auditing. Auditing is a process that assesses your company’s practices, processes, and procedures to identify areas of improvement and compliance risks. This blog explores the importance of auditing...
£33 million joint investment to boost skills, support jobs and bolster green manufacturing in UK life sciences industry
Joint government and industry investment will deliver more than 250 high-skilled jobs producing environmentally-friendly inhalers.£33 million joint government and industry investment with Kindeva will deliver more than 250 high-skilled jobs producing environmentally-friendly inhalerspackage of investment shows the government’s sustained commitment to UK life sciences as a driver of economic growth,...
Turbine Creative Helps Launch Revolutionary Web App for Chemists and Health Tech Clients
Turbine Creative’s dynamic video content showcases the future of chemical purchasing, helping propel Thermo Fisher Scientific’s Chem dex™ to new heights. Turbine Creative, a leading marketing agency renowned for its innovation and creativity, proudly continues its partnership with Thermo Fisher Scientific in supporting the launch of the groundbreaking web app,...
How to Write and Produce a Successful Business Pitch Deck
A compelling pitch deck is a powerful tool that can make or break your chances of securing funding, attracting investors, or winning new clients. It serves as a concise and visually engaging overview of your business, capturing the essence of your idea and presenting it in a way that excites...
NHS England highlights virtual wards, primary care access and command centres in winter resilience plans
NHS England’s winter resilient system roles and responsibilities plan has highlighted integrated care boards to maintain 24/7 oversight through a system co-ordination centre, the role for digital in supporting primary care access, and a target for virtual wards to maintain 80 percent occupancy rates over the winter period. Following the ‘high impact interventions’ shared by...
CE marking recognition for medical devices and in vitro diagnostics
The Medicines and Healthcare Regulatory Agency (MHRA) has released a statement on CE marking recognition for medical devices and in vitro diagnostics. The extended recognition of CE marking announced this morning does not apply to medical devices or IVDs. The government has already put in place legislation that amends The Medical Device Regulations...
