Food Safety and Standards Authority of India Blog

In today’s ever-changing world, people are more connected and informed than ever before. With social media, smart phones and various other resources, plenty of information can be obtained at a blink of an eye.However, this information is not always accurate.

Remember the super-hot social media war between Amul and Angry consumer that showed how social media can be a double-edge sword, whereby a Gurgaon resident took to Facebook to share her bizarre experience and Amul responded to clarify their side of story. 

The main cause of all this could be inexperience that hinder knowledge of what constitutes safe food. This is where FSSAI Consultant in India comes to play. Food Safety and Standards Authority of India (FASSAI) a statutory body for laying down science based standards for articles of food and regulating manufacturing, processing, distribution, sale and import of food so as to ensure safe and wholesome food for human consumption. 

It is difficult for consumers to find answer for questions like: What should one look for? What different areas are involved in food safety? Etc. making statutory bodies like Food Licensing & Registration in India paramount. Agencies like these is responsible for protecting and promoting public health through regulation and supervision of food safety, so that the end consumers don’t have to worry whether the food is safe for consumption or not.

Getting licensing from FASSAI is not an easy part, which ensures that if a product is registered under them, than it must have passed the necessary quality check before reaching you.

LAWS RELATED TO THE REGISTERATION OF GENERIC DRUGS IN INDIA.

The gubernatorial scenario associated with pharma Industry of India is changing at a very fast pace wherein DCGI is coming up with particular directives related to the narcotic policies every now and then. The documentation related to drug registration is coming at par with that off US FDA and DCGI is aimed at generating the kind of data which is acceptable on global level. The ever changing phenomenon of laws and Pharma regulatory affairs demands professional to cater the current needs of both the existing and new pharmaceutical companies to effectively launch their medicinal products in the Indian market.   

 In order to gain success by introducing a new drug it becomes imperative for the companies to minimize the time taken while launching the product in the market, as for every drug launched there are many competitors but success comes to only those companies who initiate the usage in a timely manner. Keeping this vital issue in mind RIHIM pharama has emerged as a well known Drug Regulatory Consultant in India. They assist their client in each and every process involved at various stages of product registration and approval. RIHIM has assisted several pharama manufacturers/ importers, regulators, preclinical Instruments registrations and Clinical trial companies in the process of registration with DCGI.

There are various steps for seeking permission to import or manufacture a new drug in the Indian market. Many a times the regulatory approvals often emerge as a hindrance for the firms in the introduction of a new drug in the market. To ease the complexities involved in this process there are many Drug registration consultants available in the Indian market that assist the companies starting from the registration to the launch of the medicines, clinical trials, medicinal equipments etc. There isn’t any stipulated time frame mentioned in this process which is another big issue in getting the approval on your own, therefore in-order to make the procedure of registration quick and hassle free RIHIM has their specialized team of individuals who act as per the guidelines of DCGI and get the approval faster and easier for their clients.