The global Vitamin D supplement market is projected to grow at a CAGR of 7.34% during the forecast period (2022–2027). It is segmented into two (02) product types:
- July 10, 2023 Food and Food Supplements, Regulatory Affairs
- July 10, 2023 Food and Food Supplements, Regulatory Affairs
In the food and dietary supplements industry, maintaining the highest standards of quality and safety is of paramount importance. This is where Good Manufacturing Practices (GMP) requirements come into play. GMP provides manufacturers with a framework of strict guidelines and protocols, ensuring the integrity of their products.
- July 10, 2023 Food and Food Supplements, Regulatory Affairs
The Brazilian food and dietary supplements market has undergone a period of uncertainty in recent years. However, several factors indicate its potential for growth. With a population of over two hundred and fifteen (215) million, Brazil has a large consumer base with a high purchasing power as well as a growing middle class. Consumer demand is especially prominent in niche sectors such as weight management.
- July 10, 2023 Food and Food Supplements, Regulatory Affairs
Malaysia’s food and dietary supplements market is witnessing exciting new developments, driven by growing consumer demand for health and wellness products. As more and more people embrace a proactive approach to their well-being, the industry responds with innovative launches and diverse offerings.
- July 6, 2023 Pharmaceuticals, Regulatory Labeling
The pharmaceutical industry operates in a highly regulated environment, with stringent labeling requirements and information dissemination. As pharmaceutical companies strive to meet the diverse needs of patients and healthcare professionals, managing labeling for multiple product variants becomes a critical task.
- July 5, 2023 Regulatory Affairs, Regulatory Software & Services
In today's highly regulated business landscape, organizations face the formidable challenge of managing an ever-growing volume of documents to ensure Regulatory compliance with diverse standards and regulations. To navigate through complexities such as document overload, compliance costs, increased audit scrutiny, etc., many businesses are adopting Regulatory Document Management Systems (RDMS).
- June 30, 2023 Medical Devices
Validation protocol is defined as a documented plan for testing a medical device to confirm that the production process used to manufacture the product meets the specific user, technical, and Regulatory requirements. This includes a review of process variables and operational limitations and the analysis of test results under actual use conditions.
- June 30, 2023 Publishing & Submissions, Regulatory Software & Services
The regulatory writing and publishing segment claimed a dominant 36.6% revenue share in 2022 (GVR report), propelled by outsourcing in the biopharmaceutical and medical device industries. Staying ahead in the fast-paced world of regulatory submissions is paramount. Embracing game-changing technologies and keeping updated yields faster approvals, fewer errors, and heightened Regulatory compliance.
- June 28, 2023 Medical Devices
Post-market surveillance (PMS) is a system through which surveillance of adverse events and malfunctions of health products in the post-market phase are carried out, aimed at recommending the adoption of measures to ensure the protection and promotion of public health.
- June 28, 2023 Medical Devices
Who is an IAA?
An Indian Authorized Agent (IAA) is a person, firm, or organization who has been appointed by an overseas manufacturer through a power of attorney to undertake the import of medical devices in India. The IAA collaborates extensively with manufacturers to understand their products and Regulatory needs and assist them in navigating the complex Indian Regulatory landscape.