Registration Services

Service Details:

The Bureau of Indian Standards (BIS) is the National Certification body of India that issues BIS licenses to the manufacturers and importers for various products comes under BIS voluntary or mandatory certification schemes. BIS certification is a third-party assurance of the product's quality, the consumer's security, and the trustworthiness of BIS. The government of India established the Bureau of Indian Standards under the BIS Act, 1986, under the supervision of the Indian Ministry of Consumer Protection, Food, and Public Distribution.

Being a national agency BIS has responsibility for numerous certifications for maintaining the quality standard of the products in the Indian market. The Bureau of Indian Standards grants BIS certification to companies for products that meet quality standards under the Product Certification Scheme. Furthermore, this procedure conducted through the Bureau of India Standards helps businesses to establish a brand image for their product within the industry. Over the years, the BIS has been the second name in terms of authenticity and quality. After BIS Certification, producers can use their standard marking, on their BIS-certified products.

Additional Information:

• Delivery Time: 90 days

Service Details:

The Food Safety & Standards Act, 2006 introduced to improve the hygiene and quality of food has brought about tremendous changes in the food industry. As per the Act, no person shall commence or carry on any food business except under a FSSAI license or FSSAI registration. Therefore, any food manufacturing or processing or packaging or distributing entity is now required to obtain a FSSAI License or Registration.
PROCEDURE FOR FSSAI REGISTRATION

• Documentation prior to submission of application
• Online portal generation
• Online submission of application
• Submission of (hardcopy) application to FSSAI office
• Scrutiny of application by FSSAI officials
• Inspection from FSSAI
• Grant of FSSAI Certificate

DOCUMENTS REQUIRED FOR FSSAI REGISTRATION:

• Company/ Factory registration documents
• Application form
• Manufacturing process with flow chart
• Manufacturing layout
• Scrutiny of application by FSSAI officials
• Brand certification
• esting facility

Whether your food business is food processing, trading, repacking, wholesaling, marketing, canteen or restaurant, in any case whether you are starting a food business you must have the FSSAI Licence.

Getting registration is tough due to lack of knowledge about applying correctly. We understand the whole procedure of registration & have helped hundreds of food business owner like you. We apply for FSSAI registration on your behalf & get your registration number within said time period.

Service Details:

The use of Electronic Video Games is increasing because it gives the more interaction to the user bcause it generate the visual l feedback on a two- or three-dimensional video display device such as a TV screen, computer screen or any virtual reality headset.

By considering the health of user, the Ministry of Electronic and Information Technology has made electronic video games mandatory under the Compulsory Registration Scheme.

Under this scheme Electronic Video Games are mandatory to be tested and registered as per Indian Standard IS 616: 2017 under BIS.

Aleph INDIA QMS provides the services for BIS Registration to the both manufacturers and importers of Electronic Video Games.
We guide and assist the manufacturers and importers to comply their mandatory product registration with our two verticals Aleph Industrial Corporation and Aleph Accreditation and Testing Centre.

Additional Information:

• Item Code: TrademarkRegistration
• Delivery Time: 7-15 days*
• Packaging Details: N/A

Service Details:

DRUG LICENCE : Throughout history, medical advancement has played a vital role in supporting the survival of human beings and curing life-threatening diseases. Medicine is the only weapon with mankind to fight diseases. But medicine is not an ordinary consumable product like chocolate because a particular drug can be used to cure a specific disease. Drugs should be taken with the consultation of a well-educated doctor so that he can advise about how to use when to use, what particular drug to be used to cure the disease; otherwise, it can lead to harmful side effects. The government of Indian has formed an Act which is known as “The Drugs and Cosmetics Act, 1940”. This act provides all the guidelines about the manufacturing, import, distribution, and sale of drugs and cosmetics. This act also covers all the regulations of Ayurveda, Siddha andunnai drugs.

Under “The Drugs and Cosmetic Act”, Central Drugs Standard Control Organization (CDSCO) provides the approval for drugs, clinical trials, lay down of the standards of drugs, quality control of drugs etc., with the coordination of the authority.
In December 2020, The Ministry of Health and Family Welfare published the Cosmetic rules 2020 that the licence is a must for the import of cosmetics into India.
“Drugs” - In pharmacology, a drug is a chemical substance, typically of known structure, which, when administered to a living organism, produces a biological effect.

ISSUING AUTHORITY FOR DRUG LICENCE

State Drugs Standards Control Organization (SDSCO) – State Authority with CDSCO is responsible for the grant of licence who deals in the business of Drugs & Cosmetics on the state level. The business operates in different states, drugs sold or stocked for sale in more than one state, a licence is mandatory for each location.

TYPES OF DRUG LICENCE

Drugs licence is the permission granted by the Drug controller to deal in drugs. Kinds of the licence depend upon the type of business as follows.

1. Sales Drug Licence

Types of sales Licence are as follows

1. Retail Sale Drug Licence(Chemist Shop) –
   1. Applicant premises should have an area of not less than 10sqr.mtrs.
   2. A registered pharmacist shall always be present in the store throughout working hours.
   3. Premises should have a refrigerator and air conditioner.
   1. Rent agreement
   2. Affidavit of the proprietor on stamp paper
   3. Self-attested ID proof and educational certificate
   4. Affidavit and ID Proof of registered Pharmacist
   5. Plan layout of premises in a blueprint
   6. Refrigerator Bill
   7. 5 Photographs of proprietor and pharmacist
   1. Applicant premises should have an area of not less than 15sqr.mtrs.
   2. Applicant premises must have Air conditioner and refrigerator to store the vaccines, insulin injections, sera, etc.
   3. Licence issues to the person who has degree or diploma in Pharmacy from a recognized university.
   4. A pharmacist shall be a Graduate with 1 year of experience in drug dealing.
   5. The licence shall be displayed on the premises.
Retail sale refers to the sale of the drugs to the end consumer. Retailers can sell drugs to a hospital, dispensary, medical, education, or research institutes, etc. Under the Drugs and Cosmetic Act, a drugs licence is mandatory for the retailers of drugs or Chemist shops. And a retail licence is issued by the Drug controller Authority of the State.
In case any person sells drugs without the Licence, he shall be punishable with imprisonment for the term of not less than 1 year and may extend up to 3 years with a fine up to Rs. 5000.
.Basic requirements for obtaining Retail Drug LicenceDocument requirement for obtaining Retail Drug LicenceBasic Requirements for obtaining wholesale Drug Licence

Additional Information:

• Production Capacity: Issued Licence is valid for 5 years
• Delivery Time: 30 working Days
• Packaging Details: If a retailer is indulged in the drugs business in more than 1 state, then a different license is required for the different state.