What’s happening in our world?
As a global medical consultancy, our team of experts are dedicated to sharing their expertise and knowledge, to bring excellence to the development and use of pharmaceuticals, for the advancement of human health.
As a global medical consultancy, our team of experts are dedicated to sharing their expertise and knowledge, to bring excellence to the development and use of pharmaceuticals, for the advancement of human health.
Australia continues to attract attention as a destination for early-phase and sponsor-led studies. The reasons are well understood. Faster start-up, a strong clinical research environment and a more efficient pathway into early development all make Australia commercially and operationally attractive. But choosing Australia is not the same as being ready to run well in Australia.…
Across pharma and biotech teams, the conversation is shifting. The challenge is no longer only how to respond once pressure becomes visible. It is how to build enough senior medical capacity into the model before review timelines start to slip, signatory responsibility becomes too concentrated or regional coverage becomes harder to sustain. In many teams,…
Executive Briefing · March 2026 Where Pharmaceutical Programmes Start to Slow Down Across clinical development, medical affairs and global programme delivery, one issue is showing up more consistently right now. It is rarely a lack of expertise. More often, it is a lack of alignment — and by the time it becomes visible, it is…
Dr Manuel Salgado reflects on an inspiring week at AusBiotech 2025, where innovation, collaboration and clinical excellence took centre stage. Discover his key takeaways and how My Medical Department is helping advance high-quality, patient-focused research.
Navigating the complexities of copy approval in the pharmaceutical industry is no small feat. With stringent regulations and meticulous attention to detail, companies must ensure their promotional and non-promotional materials meet the highest standards of accuracy and compliance. This article helps you navigate the complexities of copy approval.
Navigating the complexities of copy approval in the pharmaceutical industry is no small feat. With stringent regulations and meticulous attention to detail, companies must ensure their promotional and non-promotional materials meet the highest standards of accuracy and compliance. This article helps you navigate the complexities of copy approval.
Navigating the complexities of copy approval in the pharmaceutical industry is no small feat. With stringent regulations and meticulous attention to detail, companies must ensure their promotional and non-promotional materials meet the highest standards of accuracy and compliance. This article helps you navigate the complexities of copy approval.
Navigating the complexities of copy approval in the pharmaceutical industry is no small feat. With stringent regulations and meticulous attention to detail, companies must ensure their promotional and non-promotional materials meet the highest standards of accuracy and compliance. This article helps you navigate the complexities of copy approval.
Welcome to the May 2025 edition of our Regulatory Roundup! This month, we bring you the latest updates from key regulatory bodies worldwide, including the Therapeutic Goods Administration (TGA) in Australia, the U.S. Food and Drug Administration (FDA), and the European Medicines Agency (EMA). These updates highlight significant strides in medical regulation, from consultations on…
Navigating the complexities of copy approval in the pharmaceutical industry is no small feat. With stringent regulations and meticulous attention to detail, companies must ensure their promotional and non-promotional materials meet the highest standards of accuracy and compliance. This article helps you navigate the complexities of copy approval.
When it comes to the biotech industry, tax efficiency is a crucial aspect that can significantly impact a company's bottom line. For biotech firms, the journey from research and development to bringing a product to market is often long and expensive. Our latest article looks at why Australia could be an attractive destination.
Explore the future of pharmaceutical compliance in the UK and Australia, focusing on emerging regulations, technological advancements, and evolving compliance services.
Discover how My Medical Department (MMD) bridged a critical staffing gap for a leading pharmaceutical company, ensuring compliance and operational continuity during a key transition period. Learn how our expert-led, flexible support can help your team maintain high standards and efficiency.
The pharmaceutical industry operates under strict regulatory frameworks to ensure that medicines and healthcare products meet the highest standards of safety, efficacy, and compliance. Final signatories are vital in regulated markets—our latest blog delves into the UK market, highlighting the importance of support and collaboration.
Enhancing Operational Efficiency and Customer Satisfaction Through Innovative Support Solutions for a Biopharmaceutical company. This case study highlights how our team helped a leading biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines in oncology, cardiovascular, immunology, and fibrosis. Their clinical research and medical departments play a crucial role in driving the success of…