Brand communication is about conveying why a particular brand is a smarter option than the competitors in the marketplace. The Pharma industry is no oblivious to the same. Across the globe, due to the highly fragmented market space, communication becomes the whole and sole prospect to architecture any brand identity.
- July 22, 2021 Medical and Scientific Communication, Regulatory Medical Writing
- July 21, 2021 Medical and Scientific Communication, Regulatory Medical Writing
In an era of Type-Backspace-Enter, relying on the Ink-Paper-Print model especially amidst the global pandemic can be worrisome. Traditional brand communication becomes a difficult affair due to social distancing measures and hence, the society is adapting to the ‘New normal’. Brands across the globe have already adopted changing trends in communication aligning with various pandemic norms.
- July 16, 2021 Medical Devices
Bringing novel medical devices into global markets can be a daunting process for device manufacturers. As the medical device industry is highly regulated, manufacturers find it excruciating to align with the target market’s registration requirements. How to navigate the Regulatory maze of global registration requirements?
- July 15, 2021 Chemicals, Regulatory Affairs, Regulatory Labeling
Most of us have come across the terms 'Disinfectants' and 'Sanitizers' during COVID-19. Both the products fall under antimicrobial pesticides. While disinfectants and sanitizers are commonly referred as same, the major difference between them is that the disinfectants kill the microbes, bacteria and virus on the surface whereas the sanitizers reduce their numbers.
- July 15, 2021 Food and Food Supplements, Regulatory Affairs
A growing business is directly proportional to the potentiality of the market.
- July 14, 2021 Chemicals, Regulatory Artwork Services, Regulatory Affairs, Regulatory Labeling
The chemicals industry plays a pivotal role in producing petrochemicals, polymers, basic inorganics, specialities and consumer chemicals in Europe. European Chemicals Agency (ECHA) implements the EU’s chemicals legislation to protect health, safety and the environment. Classification, Labeling and Packaging (CLP) regulation helps in identifying hazardous chemicals and informs users throughout the EU about their hazards.
- July 13, 2021 Medical Devices
It is well known that the mandatory deadline for European Medical Device Regulation (EU MDR) was postponed to May 26, 2021, due to abrupt onset of COVID-19. In simple terms, the EU MDR aims to provide device clinical safety and effectiveness by establishing a robust, transparent and sustainable Regulatory framework that is recognized internationally and improves fair market access for manufacturers.
- July 13, 2021 Medical Devices
The medical devices undergo conformity assessment before they are included in the ARTG list to ensure that the devices comply with the essential principles required by the Therapeutic Goods Administration (TGA), Australia. Essential principles basically outline the safety and performance characteristics that any device should meet, so that it can be sold in Australia.
- July 13, 2021 Medical Devices
Mexico is considered as the second largest market for medical devices in Latin America. In Mexico, the Federal Commission for the Protection against Sanitary Risk (COFEPRIS) from the Secretariat of Health, regulates the Medical Device registrations and related services.
- July 8, 2021 Medical Devices, Regulatory Affairs
The Indian medical device industry has been recording significant growth and ranks in the top 20 markets for medical devices worldwide. It is estimated to reach USD 50 billion by 2025 from that of USD 10.36 billion in 2020.