Our products are currently marketed in Europe, the United States, Canada, South Africa, Brazil, and the Middle East. We provide private label distributors with documents for their country`s legal registration of our products as Over-the-counter medications without prescriptions.
The product registration documents required by most countries are:
For OTC tablets (oral solid dosage) additional test reports required are:
Please crosscheck with your country`s registration requirements if different from these, send them to us before we export your products. The minimum quantity registrable is 50,000 copies per line. Quantities less than this is not eligible. Our products are currently legalized and approved by the USA-FDA, ANVISA, EMA, HEALTH CANADA, MHRA, NMPA, PMDA, and WHO. Submit your countries requirements to our Regulatory Affairs Division via email at: QCTEAM@AMWINER.COM Please note: it is not possible to register a product without having the actual product made and tested. The test reports will be conducted after the products are made, and the documents generated from the existing product.
.We provide all the legal document required to register the products as OTC drugs products in your country. Please note our hair loss treatment products are not basic minoxidil solution with water and propylene glycol only, they are therapeutic grade products with other intermediary active pharmacological ingredients that treats other causes of hair loss, such as scalp inflammatory disorder, cicatricial disorder, hormonal changes hair loss and androgenic hair loss issues.
Raphe Pharmaceutique FDA Over the Counter (OTC) Drug Approval Consulting Services
Over the counter (OTC) drug products are defined as drug that do not require a medical prescription. They are safe and effective for use without treatment from a healthcare provider. The FDA reviews the active ingredients and labeling of these OTC drug. There are over 300,000 OTC drug products marketed in the United States. The FDA conducts a regulatory review that is based on the active pharmaceutical ingredient and labeling by therapeutic class rather than by evaluating individual drug formulations.
Firms intending to market a new product or OTC drug must submit an NDA (505) (b)(1) or 505(b)(2) application. Meeting FDA requirements can be a long process in most cases. An experienced staffs can assist you with the complicated process of submission, compliance and filing.
The two regulatory pathways for OTC drug in the United States are firstly, development under the OTC monograph process: or secondly, through the New Drug Application (NDA) process. Products that do not meeting the conditions of the OTC drug monograph must seek approval through the NDA process.
Our services as an FDA Over the Counter Drug Approval Consultants include:
Our in-house consultants work with you through all the phases of the process and ensure timely approval and marketing of your OTC product. Our compliant department is well experienced with regulatory strategies to ensure prompt and speedy FDA compliance in all phases of the approval process. We have over two decades of experience in assisting firms with the FDA approval pathway for OTC drug.
Our consultants have an in-depth understanding of FDA regulations and can determine the appropriate drug classification (monograph or ANDA) and also help prepare compliant labels according to the OTC drug monograph. What’s more, our consulting services are quicker and more cost-efficient than other firms in this domain.