How VAT Compliance Can Save Your Bottom Line
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.
Import VAT for Clinical Trials
Having a confident grasp of the essential elements of customs payments and VAT is paramount to effectively managing clinical trial budgets.
Mastering Efficiency: A Step-by-Step Guide to Centralizing Clinical Trial Procurement
Transitioning from decentralized to centralized procurement in clinical trials is not merely a procedural shift; it’s a strategic initiative. The […]
Switching from Decentralized Procurement To Centralized Procurement For Clinical Trials
Navigating the complex terrain of clinical trials, the shift from decentralized to centralized procurement emerges as a strategic odyssey. It […]
Centralized vs Decentralized Procurement for Clinical Trials: The Supply Chain’s Battle Royale
Historically, there has never been a clear winner in the battle between centralized vs decentralized procurement for clinical trials. Yet, […]
The Art of Cutting Costs: Streamlined Procurement in Clinical Trials
How can streamlined procurement reduce clinical trial overheads? Procurement costs can become a rugged terrain to navigate. Here, we identify […]
The Evolution of Clinical Trials: Navigating Centralized Procurement Trends for Efficiency and Risk Mitigation
In the world of clinical trials, the adoption of centralized procurement is gaining momentum as a strategic approach to not […]
On the Frontline of Efficiency: Contrasting Centralized and Local PPE Procurement
At the heart of a centralized procurement system lies the power to unify all purchasing operations, creating a composition of […]
Navigating the Pitfalls: Risk Mitigation in Centralized Procurement for Global Decentralized Trials
Picture this: A decentralized clinical trial that mitigates risks, cuts costs, and enhances ethical compliance. Well, that dream can become […]
Racing Against Time: SIV Date in 2 Weeks – Fast-Track IOR Solutions
In a race to beat the clock, a pharmaceutical giant faced a critical challenge, the urgent import of Patient Recruitment […]
How to Set Up Your Inventory Management System
Why inventory management systems? A major side effect of the pandemic has been the swift adoption of direct-to-patient and virtual […]
The Rise of Centralized Procurement in Healthcare
Centralized procurement involves making all purchasing decisions through a single, dedicated organization or team. Here we explore the significance of […]
Extracting Crucial Patient Data from a Conflict Zone | Ukraine Medical IOR
The Fundamentals: Return a shipment of eCOA devices from Ukraine to the UK for a global CRO. The Complexities: Navigating […]
Streamlining Clinical Trial Project Management: The Imperative of Centralized Global Trials
In the evolving realm of healthcare and pharmaceuticals, the clinical trial journey is a linchpin in introducing innovative treatments and […]
FAQs: What is an EOR, Why Do I Need One for Clinical Trial Exports, and More
Clinical trials are conducted in multiple countries around the world. In 2021, over 288,000 clinical trials were active worldwide, with […]
The Vital Role of Importers of Record in Ensuring VAT Compliance in Global Clinical Trials
Global clinical trials are critical for advancing medical research and developing life-saving treatments. However, conducting these trials across international borders […]
What is an Importer of Record (IOR)? And Other Frequently Asked Questions.
The Importer of Record (IOR) is an integral part of the global supply chain management for clinical trials. The IOR […]
Streamlining the Clinical Trial Supply Chain: Ensuring Innovation Efficiency
Clinical trials are essential for developing new medicines and getting them to patients who need them. They help bridge the […]
From Aztec to Algorithm: Innovations in Mexican Clinical Research
Mexico has become an important part of global clinical trials. It provides a favorable environment for conducting medical research. The […]
Taj Mahal of Trials: India’s Clinical Research Powerhouse
The landscape The sheer volume of trade in India is one of the standout features of the region. As one […]
What is an Importer of Record (IOR)? A Comprehensive Guide for Importing Goods
What is the Definition of an Importer of Record(IOR)? The importer of record (IOR) is the entity that is legally […]
From Customs Clearance to Quality Control: Importing Clinical Trial Products to Sweden
Sweden has a robust regulatory framework for clinical trials, which creates hurdles for sponsors and CROs looking to import trial […]
The French Connection: Challenges and Opportunities in the French Clinical Trial Arena
France has long been a hub for clinical research, with a well-established and highly regulated clinical trial landscape widely respected […]
Going Dutch: Navigating Import Compliance in the Netherlands
The Netherlands is a major international trade and commerce gateway with a highly developed import and customs landscape. The country […]
Stars, Stripes, and Clinical Trials: Navigating US Import Challenges
The United States of America is a leading country in the clinical trial landscape and for new drug developments. With […]
Tree of Life: Singapore’s Lush Clinical Trial Space
Singapore has emerged as a top destination for clinical trials due to its advanced healthcare infrastructure, favorable regulatory environment, and […]
The Trials of the Nile: Importing Challenges Facing Clinical Trials in Egypt
The MENA (Middle East and North Africa) region offers significant opportunities for new drug development due to its large patient […]
Delays Down Under: Overcoming Australia’s Clinical Trials Challenges
Australia’s position as a major economic player on the world stage is unique due to its geographical isolation and strong […]
From Samba to Science: Conquering the Import Challenges for Clinical Trials in Brazil
Clinical trials are essential to drug development and must be conducted in compliance with regulations and standards that ensure patient […]
The Great Wall of Regulations: Overcoming Import Challenges for Clinical Trials in China
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.
Top 6 Trends Predicted to Impact Clinical Trials in 2023
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.
Five Challenges Facing Contemporary Clinical Trials
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.
The TecEx Medical Solution in Argentina
Shipping into Argentina is notorious for its complex customs requirements and lengthy lead times to import trial supplies into the country.
9 Latest Medical Technologies for 2022
Every year, there are new technologies emerging that are revolutionizing healthcare, and old technologies that are being advanced further.
Bringing Healing to An Ailing System – The Age of Globalized Healthcare
When considering the topic of contemporary healthcare, there exists an optimistic assumption that a globalized world gives rise to worldwide resources.
What is AI in Healthcare?: An Overview for Beginners
Artificial Intelligence (AI) is increasingly being used in healthcare for a wide range of applications.
The Rise of Climate-Smart Healthcare
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.
What is Digital Transformation in Healthcare? A 2022 Guide
Digital transformation has been slowly changing the healthcare industry for decades. But the arrival of COVID-19 accelerated this rapidly.