Drug manufacturing federal requirements
If you own or operate a drug or pharmaceutical manufacturing establishment, you are required to register it with the Food and Drug Administration (FDA) within five days after starting operations. According to the FDA, a drug manufacturer is anyone who is engaged in manufacturing, preparing, propagating, compounding, or processing (which includes packaging, repackaging, or relabeling, among other things) of a prescription drug. Registration information must be submitted electronically (unless a waiver is granted).
As part of the registration process, you must list each drug manufactured by your company that is intended for commercial distribution and submit this information to the FDA twice a year, in June and December, and notify the agency if any information has changed.
Registration information must be renewed annually. The renewal period occurs between October 1 and December 31. However, listing updates can occur at any time during the year.
If your business involves controlled substances, you are subject to additional requirements. For example, if you distribute, store, or manufacture a named controlled substance, you must apply for a federal controlled substances registration issued by the Drug Enforcement Agency (DEA). A separate DEA registration is also required for each place of business or practice at a physical location where controlled substances are manufactured, distributed, imported, exported, or dispensed by a person. This registration is also subject to annual renewal.
State requirements for business licenses
A drug manufacturing license is required at the state level. These laws and license types vary from state to state. For example, depending on your state, you may need a manufacturer license, wholesale distributor license, or pharmacy facility license.
If you deal with controlled substances, separate state licensing and permit requirements exist.
When applying for a drug manufacturer license, you must provide the following information:
- Proof of FDA drug establishment registration
- Corporate documents
- Certificate of Good Standing
- Proof of registered agent
- Information on owners and officers
- Facility plans or construction drawings
- Description of security system and security measures in place
- Facility manager information
- Self-inspection report
- List of drugs to be manufactured/repackaged
- Copy of VAWD (Verified-Accredited Wholesale Distributors) certificate
- Lease/zoning statement
- Certificate of Occupancy
- Certificate of insurance
Before a license is issued, the state could also require a facility inspection.
State licensing requirements for virtual manufacturers
Many states require licensure of virtual manufacturers. A virtual drug manufacturer sells prescription drugs, products, and/or devices under its own label but outsources the actual manufacturing and distribution process.
Many states include virtual manufacturers in the same compliance bucket as wholesalers. These licensing requirements can be very specialized, and you may choose to request certain exemptions.
Licensing requirements for change of ownership
If your business undergoes a change of ownership, depending on the state in which you operate, you may be required to notify the appropriate pharmacy board of the change.
To continue operations, some states also require an application for a new license. If the application is received within a certain timeframe, the facility can typically continue operating until the new license is issued.
However, there are exceptions, and some states do not allow continued operations after closure of the original business or change of ownership if the application is pending.
Because these laws are complex and vary, it’s best to consult a legal services provider who can identify the actions your company must take in accordance with regulations and guide you through the process.
Do cosmetic manufacturers need a drug manufacturing license?
Certain cosmetic products meet the definition of both cosmetics and drugs. This generally happens when a product has two intended purposes. For example, an anti-dandruff shampoo is considered a drug since it’s a dermatological treatment. This is also the case with toothpaste, deodorants that contain antiperspirants, moisturizers and makeup advertised with sun protection claims. Such products must comply with registration and licensing requirements for drugs and cosmetics.
CT Corporation can help
CT Corporation can help you stay up to date with changing requirements and forms so you can focus on running a successful drug or pharmaceutical manufacturing business. We complete license applications efficiently and correctly, so you don’t spend time chasing down the proper licenses. Once your drug manufacturing license has been issued, we ensure that you remain compliant will all licensing laws.
To learn more about how CT Corporation can help you manage your business licensing needs, contact a CT Corporation Service Representative.
