Synopsis
0
KDMF
0
VMF
0
Canada
DRUG PRODUCT COMPOSITIONS
0
FDF
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
API SUPPLIERS
Suanfarma, at the Core of a Better Life.
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
CEP/COS
NDC
ASMF
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
Jai Radhe Sales is your partner for all your sourcing needs.
HRV Global Life Sciences - Market Expansion Leader in Pharmaceuticals.
Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Mesochem is focused on incessant innovation along with the R&D of new APIs.
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
USDMF
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]CEP/COS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results] EU WC
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]NDC API
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Listed Suppliers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]API Reference Price
API/FDF Prices: Book a Demo to explore the features and consider upgrading later
API Imports and Exports
Drugs in Development
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]INTERMEDIATE SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]FDF Dossiers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]FDA Orange Book
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Europe
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Australia
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Related Excipient Companies
SPI Pharma
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Faran Shimi Pharmaceutical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Gangwal Healthcare
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Nanjing Well Pharmaceutical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Pfanstiehl
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Actylis
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Anhui Sunhere Pharmaceutical Excipients Co.,Ltd
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]DFE Pharma
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Gangwal Chemicals
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Ideal Cures Pvt Ltd
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Ingredion Pharma Solutions
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Kerry
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Microlex e.U
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Pharmatrans-Sanaq
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Pluviaendo
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Prachin Chemical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Roquette
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Seppic
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Shanghai Shenmei Pharmaceutical Technology Co., Ltd
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Sigachi Industries
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Fillers, Diluents & Binders
Disintegrants & Superdisintegrants
Direct Compression
Co-Processed Excipients
Thickeners and Stabilizers
Granulation
Lubricants & Glidants
Taste Masking
Coating Systems & Additives
Controlled & Modified Release
Chewable & Orodispersible Aids
Emulsifying Agents
Parenteral
Film Formers & Plasticizers
API Stability Enhancers
Rheology Modifiers
Digital Content
NEWS #PharmaBuzz
Global Sales Information
US Medicaid Prescriptions
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Market Place
APIs
Reply
31 Oct 2024
Reply
24 Jul 2024
Reply
09 Jul 2024
Reply
06 Jun 2023
Reply
01 Sep 2021
Reply
18 Jun 2020
Reply
22 Jan 2020
Reply
12 Dec 2019
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
33
PharmaCompass offers a list of Clomiphene Citrate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Clomiphene Citrate manufacturer or Clomiphene Citrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clomiphene Citrate manufacturer or Clomiphene Citrate supplier.
PharmaCompass also assists you with knowing the Clomiphene Citrate API Price utilized in the formulation of products. Clomiphene Citrate API Price is not always fixed or binding as the Clomiphene Citrate Price is obtained through a variety of data sources. The Clomiphene Citrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fertyl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fertyl, including repackagers and relabelers. The FDA regulates Fertyl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fertyl API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Fertyl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fertyl supplier is an individual or a company that provides Fertyl active pharmaceutical ingredient (API) or Fertyl finished formulations upon request. The Fertyl suppliers may include Fertyl API manufacturers, exporters, distributors and traders.
click here to find a list of Fertyl suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Fertyl DMF (Drug Master File) is a document detailing the whole manufacturing process of Fertyl active pharmaceutical ingredient (API) in detail. Different forms of Fertyl DMFs exist exist since differing nations have different regulations, such as Fertyl USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Fertyl DMF submitted to regulatory agencies in the US is known as a USDMF. Fertyl USDMF includes data on Fertyl's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Fertyl USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Fertyl suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Fertyl Drug Master File in Japan (Fertyl JDMF) empowers Fertyl API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Fertyl JDMF during the approval evaluation for pharmaceutical products. At the time of Fertyl JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Fertyl suppliers with JDMF on PharmaCompass.
A Fertyl CEP of the European Pharmacopoeia monograph is often referred to as a Fertyl Certificate of Suitability (COS). The purpose of a Fertyl CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Fertyl EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Fertyl to their clients by showing that a Fertyl CEP has been issued for it. The manufacturer submits a Fertyl CEP (COS) as part of the market authorization procedure, and it takes on the role of a Fertyl CEP holder for the record. Additionally, the data presented in the Fertyl CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Fertyl DMF.
A Fertyl CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Fertyl CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Fertyl suppliers with CEP (COS) on PharmaCompass.
A Fertyl written confirmation (Fertyl WC) is an official document issued by a regulatory agency to a Fertyl manufacturer, verifying that the manufacturing facility of a Fertyl active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Fertyl APIs or Fertyl finished pharmaceutical products to another nation, regulatory agencies frequently require a Fertyl WC (written confirmation) as part of the regulatory process.
click here to find a list of Fertyl suppliers with Written Confirmation (WC) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Fertyl as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Fertyl API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Fertyl as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Fertyl and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Fertyl NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Fertyl suppliers with NDC on PharmaCompass.
Fertyl Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Fertyl GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Fertyl GMP manufacturer or Fertyl GMP API supplier for your needs.
A Fertyl CoA (Certificate of Analysis) is a formal document that attests to Fertyl's compliance with Fertyl specifications and serves as a tool for batch-level quality control.
Fertyl CoA mostly includes findings from lab analyses of a specific batch. For each Fertyl CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Fertyl may be tested according to a variety of international standards, such as European Pharmacopoeia (Fertyl EP), Fertyl JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Fertyl USP).
Comment (2)
