Global logistics and customs compliance issues do not have to be your burden while trying to manage a clinical trial. […]
With an epidemic proportion of obesity growing, prominent financial researchers predict the obesity drug category will exceed $100 Billion by […]
COVID-19 brought the world to a standstill. It emptied out streets, cleared out offices, grounded the travel industry, shut down […]
Forget crash diets and fad workouts. The hottest trend in Hollywood isn’t a new juice cleanse. It’s a prescription medication […]
VAT compliance is a critical aspect of conducting global clinical trials successfully. Collaborating with a medical Importer of Record is pivotal in ensuring compliance with VAT regulations and other import-related tax requirements.
Having a confident grasp of the essential elements of customs payments and VAT is paramount to effectively managing clinical trial budgets.
Transitioning from decentralized to centralized procurement in clinical trials is not merely a procedural shift; it’s a strategic initiative. The […]
Navigating the complex terrain of clinical trials, the shift from decentralized to centralized procurement emerges as a strategic odyssey. It […]
Historically, there has never been a clear winner in the battle between centralized vs decentralized procurement for clinical trials. Yet, […]
How can streamlined procurement reduce clinical trial overheads? Procurement costs can become a rugged terrain to navigate. Here, we identify […]
In the world of clinical trials, the adoption of centralized procurement is gaining momentum as a strategic approach to not […]
At the heart of a centralized procurement system lies the power to unify all purchasing operations, creating a composition of […]
Picture this: A decentralized clinical trial that mitigates risks, cuts costs, and enhances ethical compliance. Well, that dream can become […]
In a race to beat the clock, a pharmaceutical giant faced a critical challenge, the urgent import of Patient Recruitment […]
Why inventory management systems? A major side effect of the pandemic has been the swift adoption of direct-to-patient and virtual […]
Centralized procurement involves making all purchasing decisions through a single, dedicated organization or team. Here we explore the significance of […]
The Fundamentals: Return a shipment of eCOA devices from Ukraine to the UK for a global CRO. The Complexities: Navigating […]
In the evolving realm of healthcare and pharmaceuticals, the clinical trial journey is a linchpin in introducing innovative treatments and […]
Clinical trials are conducted in multiple countries around the world. In 2021, over 288,000 clinical trials were active worldwide, with […]
Global clinical trials are critical for advancing medical research and developing life-saving treatments. However, conducting these trials across international borders […]
The Importer of Record (IOR) is an integral part of the global supply chain management for clinical trials. The IOR […]
Clinical trials are essential for developing new medicines and getting them to patients who need them. They help bridge the […]
Mexico has become an important part of global clinical trials. It provides a favorable environment for conducting medical research. The […]
The landscape The sheer volume of trade in India is one of the standout features of the region. As one […]
What is the Definition of an Importer of Record(IOR)? The importer of record (IOR) is the entity that is legally […]
Sweden has a robust regulatory framework for clinical trials, which creates hurdles for sponsors and CROs looking to import trial […]
France has long been a hub for clinical research, with a well-established and highly regulated clinical trial landscape widely respected […]
The Netherlands is a major international trade and commerce gateway with a highly developed import and customs landscape. The country […]
The United States of America is a leading country in the clinical trial landscape and for new drug developments. With […]
Singapore has emerged as a top destination for clinical trials due to its advanced healthcare infrastructure, favorable regulatory environment, and […]
The MENA (Middle East and North Africa) region offers significant opportunities for new drug development due to its large patient […]
Australia’s position as a major economic player on the world stage is unique due to its geographical isolation and strong […]
Clinical trials are essential to drug development and must be conducted in compliance with regulations and standards that ensure patient […]
What makes importing clinical trial goods into China so difficult? Simply put, not all import destinations are created equally. Due to multiple factors, some destinations are infinitely more difficult than others. Here are some reasons why China, as one of these challenging destinations, is so tricky to navigate.
TecEx Medical has observed industry interest in readily adopting new technologies and methods to overcome obstacles in the clinical trial life cycle. We have curated a list of top trends expected to impact trials in 2023.
The clinical trial space is notoriously difficult – it’s like trying to climb an impossibly difficult mountain that gets steeper and steeper without a summit.
Shipping into Argentina is notorious for its complex customs requirements and lengthy lead times to import trial supplies into the country.
Every year, there are new technologies emerging that are revolutionizing healthcare, and old technologies that are being advanced further.
When considering the topic of contemporary healthcare, there exists an optimistic assumption that a globalized world gives rise to worldwide resources.
Artificial Intelligence (AI) is increasingly being used in healthcare for a wide range of applications.
In the age of globalized healthcare, there is a seismic shift in the way we view fundamental features of the medical industry as a whole.
Digital transformation has been slowly changing the healthcare industry for decades. But the arrival of COVID-19 accelerated this rapidly.