Articles in the IP and Regulatory Affairs Category
Clinical Research Organisations, Featured, Headline, IP and Regulatory Affairs, Interactive Career Sharing Session »
A Contract Research Organization is a service organization that provides support to the pharmaceutical/biotech industry. CROs provides clients a wide range of “outsourced” pharmaceutical research services to aid in the drug and medical device research & development process.
Services offered by CROs include: product development, formulation and manufacturing; clinical trial management (preclinical through phase IV); clinical, [...]
IP and Regulatory Affairs »
We all talk about protecting IP, but how much do we actually know?
There are many ways to protect your intellectual property. To name the relevant list for BMS and business practices, they are:
1. Patents
2. Copyright
3. Registered designs
4. Trade marks
5. Layout-designs of integrated circuits
Certain protections need to be filed and applied while others don’t.
IP protections that [...]
IP and Regulatory Affairs »
Simply explained, the “Publish or Perish” syndrome is faced by many researchers and academia all over world. It is true that publishing research findings is an important part of any researcher’s work as it involves the recognition of their work thus determining their career. However, we must not forget that not being able to publish does [...]
IP and Regulatory Affairs »
When joining the Biomedical Sciences sector, it is essential to understand the industry itself. BMS is a dynamic and fast paced industry which is diverse in its political systems, culture and economic development. A strong and fast growing industry that has the capability of driving a country’s economy cannot be left unregulated. Regulations plays an [...]
