Find Approval Services for all your Approval needs!
For more information, call 1-403-770-1994 or email us
Global Regulatory
The International Regulatory Outsourcing Network.
08 September 2010

Account Management

Welcome!
You are not logged in.

Regulatory Consulting
Regulatory Requests
 
Find Approval regulatory consultants for all your Approval consulting, audits and training such as regulatory submissions, regulatory compliance, advisory meetings, validation, regulatory actions, warning letters, import detentions, exporting, importing, seizures, non-approvals, FDA, Good Manufacturing Practices in countries such as the USA, Canada, Mexico, European Union, United Kingdom, Ireland, China, Japan, Australia, etc.

Approval Requests for Proposals

Global Regulatory.com has received the following incoming Approval Requests which need to be fulfilled ! These Approval Requests are received from a variety of sources ranging from start-up companies to large, multinational corporations actively seeking companies to perform their Approval services. If your company receives requests that it can not fulfill, please refer them to us! If you have questions, please e-mail us or call 403-770-1994 .
Incoming Approval Requests
#
Approval request description
status
10-00120 Regulatory Company needed for EC, AEMPS submissions for approval of clinical study approximately 3 sites in Spain ( read more ).....
10-00117 CRO needs regulatory consultant for Anvisa approval of facility. ( read more ).....
10-00091 Beverage Manufacturer needs Food Regulatory Consultant for Country by country approval for importation and distribution of beverage products ( read more ).....
10-00069 Medical Device Manufacturer needs FDA Regulatory Consultant for 510K approval Classification Panel: Radiology Diagnostic Devices Classification name: Positron Camera, Class I, 21 CFR § 892.1110 Pr ( read more )..... Closed
10-00025 Import and Export Consultant needed to advise on import of an equine and human nutraceutical from the usa. Both products are manufactured in fda approved labs but do not have fda approval as of yet. T ( read more )..... Closed
10-00010 Middle East Regulatory Consultant needed for Facility Design and Saudi FDA approval ( read more )..... Closed
10-00005 South Africa Regulatory Consultant need to adcise on obtainings approvals to market dietary supplements or nutraceuticals ( read more )..... Closed
09-0179 FDA Medical Device Consultant needed for FDA PMA, 510(k) Approval Training ( read more )..... Closed
09-0177 India Pharmaceuticals mfg needs regulatory consultant for Turkey MOH,Uk-MHRA and AUTGA and Afssaps MCC south Africa and Health Canada Approvals ( read more )..... Closed
09-0175 Medical Device Consultant needed for Pre market Approvals for Class I, II, III, Medical Devices For USA, Europe, Canada ISO 13485:2003 CMDCAS Implementation ISO Training Trade Complaint Handling ( read more )..... Closed
09-0172 Dusk mask (Disposable mask & Changeable cartridge and face piece) manufacturer in Korea, need OSHA consultant to assist on NIOSH certification. Since it is first time and we don't know much about the ( read more )..... Closed
09-0168 Experienced Regulatory consultant needed to help obtain a generic animal drug approval. The consultants need to have experience and should indicate how much they charge for your services as well as ot ( read more )..... Closed
09-0156 Texas Cookware Exporter needs Regulatory Advisor to advise on The Turkish Governments "Safety Approval" Process. The Turkish Goverment requires all consumer products imported into their country recei ( read more )..... Closed
09-0129 USDA approval expert required for helping writing a development plan and consulting on other regulatory issues. We have an exciting immunomodulator product for animal health that we are ready to devel ( read more )..... Closed
09-0119 Regulatory consultant needed in Italy to obtain Italian Azienda di Sanita Locales (ASLs)approvals in the regions of Lombardia, Piedmonte, and Emilia-Romagna so that we can expand our healthcare screen ( read more )..... Closed
09-0039 US FDA Pharmaceutical Consultant needed for fda registration approval to operate a warehouse and distribution site for pharmaceutical product handling ( read more )..... Closed
09-0026 US Pharmaceutical Manufacturer needs Pharmaceutical Consultant to provided FDA regulatory help with OTC pharmaceutical filing, labelling, review, approval, labelling requirements and other issues re ( read more )..... Closed
09-0015 India Export Manufacturer needs regulatory consulting firm to assit in ANVISA approval for manufacturing plant located in India. ( read more )..... Closed
08-0173 Pharmaceutical Legal or Regualtory Consultant needed to prepare a written regulatory opinion, outlining the regulatory path requirements and time-line to obtain marketing approval for topical product ( read more )..... Closed
08-0156 Medical Device Manufacturer needs Medical Device COnsultant to assist in 510K pathway with a device that is very similar to several devices approved by the FDA. I am also looking into European approv ( read more )..... Closed
08-0149 Regulatory Consultant needed in Jordan which can give the regulatory service (compile the Dossier as required by JOrdan FDA, submit & follow up the Dossier with JOrdan FDA. Obtain the registration app ( read more )..... Closed
08-0121 India pharmaceutical company planning to submit applications for approval from MHRA, MCC & TGA are seeking competent Regulatory Consultants to assist us in successfully file our applications. ( read more )..... Closed
08-0118 India Pharmaceutical Manufacturer needs FDA medical device regulatory consultant to assist on 510(k) Approval ( read more )..... Closed
08-0105 Food Manufacturer needs spanish speaking food regulatory consultant needed for translation of food product labels from English to Spanish as well as help in navigating Mexican import laws and in obtai ( read more )..... Closed
08-0101 Medical Device Consultant needed to submit an SFDA for product approval of implantable orthopedic products(medical devices) ( read more )..... Closed
08-0083 Pharmaceutical Regulatory Consultants with experience in US IND Maintenance needed to introduce Change Control Procedures (CCP) to R&D line functions to assure compliance with the requirements at 21CF ( read more )..... Closed
08-0076 Consultant for regulatory approval for the Pharmaceutical Formulation Products in overseas contraries. [Particularly African countries]Country wise requirement of the manufacturing setup and product ( read more )..... Closed
08-0074 Pharmaceutical Regulatory Consultant needed to conduct initial GMP/GLP mock inspection, advice on corrections necessary to ensure FDA approval, and then submission of ANDA for a generic drug. ( read more )..... Closed
08-0047 Dietary Supplement Manufacturer needs Regulatory Consultant to file Regulatory Request for Approval of supplement for export to Mexico ( read more )..... Closed
08-0038 FDA Food Consultant needed for consulting regarding FDA approval for ice and water beverage. ( read more )..... Closed
08-0036 WHO GMP Pharmaceutical Manufacturers needs pharmaceutical regulatory consultant to go for USFDA approval of our Manufacturing plants and register both OTC & Generic Formulations. ( read more )..... Closed
08-0030 Regulatory consultant needed for company seeking FDA approval for healing water beverage and Ice ( read more )..... Closed
08-0027 Food Regulatory Consultant / Expert needed in CFSAN and requirements to qualify a plastic for intended food contact. Manufacturer seeks approval for new resin. ( read more )..... Closed
08-0016 FDA Regulatory Consultant needed for assisting in getting a medical device product approved. It may be under an HDE or possibly grandfathered. However a 510k Approval would be preferred. ( read more )..... Closed
08-0013 Pharmaceuticals Regulatory Consultant needed to determine if it is feasible to extend plans for a trial into Belize, Costa Rica, Dominican Republic, and Virgin Islands. We need to know how long it wil ( read more )..... Closed
08-0012 Regulatory Consultant needed to consult on distributing medical products in the Middle East. Do I need to get any documents before doing the trading business? What kinds of regulatory that I should sa ( read more )..... Closed
08-0004 Attorney representing a pharmaceutical company in a dispute with a manufacturer here in the Superior Court of San Diego County. I am interviewing potential expert consultants/witnesses to provide tes ( read more )..... Closed
08-0003 FDA Pharmaceutical Regulatory Consultant needed for ANDA preparation and submission. Consultant must have experience with FDA and must have been successful on gaining approval on FDA submissions. ( read more )..... Closed
08-0002 Urgent 3 month need for experienced Japanese Consultants (x2)to assist with a Global Compliance project Post-approval Compliance - Japanese Regulations & Directives expertise. GMP, CMC & compliance e ( read more )..... Closed
07-0121 Cosmetics Regulatory Consultant needed to assist with approval of a new cosmetic ingredient into Japan/China. ( read more )..... Closed
07-0116 Need management services for completion of EPA registration of disinfectant product. After completion of EPA registration, will need to manage all FDA required tests and studies needed for approval o ( read more )..... Closed
07-0113 Regulatory consultants needed to provide regulatory strategy and approval pathway for switch from approved iv formulation to an oral formulation. Prior successful experience in this area preferred. ( read more )..... Closed
07-0089 Pharmaceutical consultant needed to represent client at MOH meetings, discuss optimal strategy for registration of pharmaceuticals with MOH;hands on activities with respect to dossier compilation and ( read more )..... Closed
07-0088 Regulatory consultatnt needed for assistance with obtaining regulatory approval in Korea. Our products is cleared by FDA and health Canada. Also CE marked. ( read more )..... Closed
07-0081 Pharmaceutical regulatory consultant needed to assist in understanding of exact regulatory process for applying for and obtaining marketing authorization and approval ( read more )..... Closed
07-0073 Generic Pharmaceutical Manufacturer needs registration and approval consulting for Active Ingredients and Finished Dosage Forms in Japanese market. In this connection we would like to know the sched ( read more )..... Closed
07-0071 Manufacturer of HDPE bottles needs an FDA pharmaceutical consultant who can file USFDA Drug Master File and get vendor approval for from us fda. We prefer consultant from india ( read more )..... Closed
07-0070 Medical device manufacuter seeks consultant for gaining clearance in Canada for device with 510(k) clearance and CE approval ( read more )..... Closed
07-0038 Technology Transfer Office needs EU approval advisory services for biological product which is produced in China. The biological product has been market in China India,Philippine and other several co ( read more )..... Closed
07-0035 Regulatory consultant needed with experience in the regulatory approval of nutraceuticals and supplements in the USA ( read more )..... Closed
07-0033 Pharmaceuticals Consulting Firm needed for Fast track approval or orphan drug approval. Drug registration approval in country specified. Import of unregistered drug in those countries. ( read more )..... Closed
07-0030 Regulatory/Clinical support needed for Dermal Filler FDA PreMarket Approval PMA ( read more )..... Closed
07-0029 Regulatory consultant needed for UK MHRA approval for our pharmaceutical formulation manufacturing unit. ( read more )..... Closed
07-0024 Pharmaceuticals Regulatory Consultant needed for assisting on MHRA approval for pharmaceutical preparations plant. ( read more )..... Closed
07-0004 Pharmaceuticals company needs regulatory consultant to provide comprehensive product-registration services and requirements right from product development , registration and regulatory approval of pha ( read more )..... Closed
06-0159 Medical Device Consultant needed who is familiar with medical device regulations in South Africa and who can assist in getting approval for registering and marketing there. ( read more )..... Closed
06-0152 GMP consultant needed to support a Japanese company in cGMP regulations in preparation for a pre-approval inspection PAI ( read more )..... Closed
06-0126 Regulatory consultant needed for advising on FDA CVM Drug Approval and Clinical Trial for cancer treatment for canines using a autologous cell based product ( read more )..... Closed
06-0104 Regulatory consultant experienced with combination products (medical devices/pharmaceuticals) approval process in the UK needed for providing outline of regulatory approval process. ( read more )..... Closed
06-0103 Larg manufacturer needs regulatory consultants for USA & Canada Cosmetics and Dietary Supplement registration, product assessments and Technological consultation. We need your consultancy in the pro ( read more )..... Closed
06-0102 Sponsor needs consultants for preparing Annual Product Reports, Product Renewals and post-approval submissions in CTD format ( read more )..... Closed
06-0098 Consultant needed for approval of application to export bottled water to UK in complaince with the UK Food Standards Agency ( read more )..... Closed
06-0096 Regulatory ocnsulting needed for obtaining US FDA and Health Canada approval for novel oral and topical nutraceutical/cosmeceutical. We have recently been awarded a US utility patent for the world's ( read more )..... Closed
06-0095 Pharmaceuticals regulatory consultant wanted for US FDA ANDA approval of pharmaceutical tablets as well as preparation of GMP manufacturing facility. ( read more )..... Closed
06-0094 Manufacturers of pharmaceuticals hard gel capsules needs pharmaceutical regulatory consultant for european registration, auditing, and filing an EDMF for approval to market product in Europe. ( read more )..... Closed
06-0083 Medical Device Manufacturer of active implantable devices seeks consultant to advise on regulatory approval process in Australia. ( read more )..... Closed
06-0081 Medical Device regulatory and translation services needed for approval and guidance on OTC Oral Health Products. Translation into 17 EU official languages including allowable claims and required text ( read more )..... Closed
06-0061 Regulatory consultant fluent in Spanish needed for consulting on US FDA approval process for injectable veterinary drug products. ( read more )..... Closed
06-0057 Seasoned high level regulatory pharmaceuticals professional with expertise in parenterals, sustained release injectable dosage forms for development of NDA strategy and to assess : 1. Aseptic facili ( read more )..... Closed
06-0038 Medical Device manufacturer needs consultants to assist with FDA medical device registration and approval filings for medical tubing for IV solution bags and lay flat tube Consulting needed to guide ( read more )..... Closed
06-0033 Medical Device manufacturer of non-invasive devices currently in clinical studies needs regulatory consulting for approval and marketing of the devices. ( read more )..... Closed
06-0025 US FDA medical device consultant needed for evaluation of FDA registration and approval filing requirements for in-vitro diagnostic whole blood testing kit for clotting time. The kit contains 3 diffe ( read more )..... Closed
06-0014 API manufacturer needs USFDA Regulatory Consultant well versed with FDA regulations for approval of Active Pharmaceutical Ingredient (API) facility by USFDA Authorities in India. It is a green field ( read more )..... Closed
06-0003 US FDA Medical Device Consultant needed for FDA approval for a low level laser ( read more )..... Closed
06-0001 Experienced US FDA Medical Device Consulant needed for filing Medical Device 510(K) including collecting related information, pick SE predictive device, and are experieced in geting approval from FDA ( read more )..... Closed
05-0062 Experienced US FDA Biopharmaceutical Regulatory Consultant needed for foreign biopharmaceutical company entering US. Consultant will provide guidance for regulatory process required to get FDA approva ( read more )..... Closed
05-0061 Regulatory clinical trials consultant needed for consulting on guidelines and approvals to conduct a clinical study for natural nutraceuticals ( read more )..... Closed
05-0026 Pharmaceutical Regulatory Consultant needed as a Liasoning Officer to get Medicinal formulation register in South East Asian countries. We are R&D organization , with company registered in Germany. We ( read more )..... Closed
05-0023 Regulatory consultant needed for consulting on registrations and approvals of dietary supplements for sale in HK and TW"" ( read more )..... Closed
05-0004 FDA Medical Device Regulatory Consultants needed for FDA PMA or 510K protocol approvals for latex male and female condoms. ( read more )..... Closed

For more information on Approval services, please call 1-403-770-1994 or email us

Approval Related News
FDA Approves First Generic Enoxaparin Sodium Injection
2010-07-23 00:00:00
The U.S. Food and Drug Administration today approved the first generic vers... 

Press Release
2008-02-06 00:00:00
The U.S. Food and Drug Administration today announced its intention to take... 

Press Release
2008-02-06 00:00:00
The U.S. Food and Drug Administration today approved the first generic vers... 

Press Release
2008-02-04 00:00:00
The U.S. Food and Drug Administration, part of the U.S. Department of Healt... 

Press Release
2008-02-01 00:00:00
The U.S. Food and Drug Administration today approved the Endeavor Zotarolim... 

Press Release
2008-01-17 00:00:00
The U.S. Food and Drug Administration today approved the first clotting sol... 

Press Release
2008-01-16 00:00:00
On Jan. 2, the U.S. Food and Drug Administration (FDA) expanded the indicat... 

Press Release
2008-01-14 00:00:00
Drug currently approved for use in treating some forms of multiple sclerosi... 

Press Release
2008-01-14 00:00:00
Industry Seeks Normalization of Trade in Agricultural Biotechnology WAS... 

Press Release
2007-12-28 00:00:00
These products are illegal drugs and contain undeclared active ingredients ... 

Press Release
2007-12-27 00:00:00
This press release contains a revision posted Dec. 28, 2007, to correct the... 

Press Release
2007-12-19 00:00:00
The U.S. Food and Drug Administration's (FDA) Office of Criminal Investigat... 

Press Release
2007-12-18 00:00:00
Action is part of President's Emergency Plan for AIDS Relief The U.S. Fo... 

Press Release
2007-12-03 00:00:00
The U.S. Food and Drug Administration today announced a new e-mail service ... 

Press Release
2007-11-21 00:00:00
The U.S. Food and Drug Administration has approved tablet, chewable tablet,... 

Press Release
2007-11-19 00:00:00
Registration Facilitates Market Acceptance in France Ann Arbor , MI -... 

Press Release
2007-11-19 00:00:00
The U.S. Food and Drug Administration today announced that it has approved ... 

Press Release
2007-11-09 00:00:00
The Food and Drug Administration (FDA) has approved Zyrtec-D (cetirizine HC... 

Press Release
2007-11-01 00:00:00
Some lacked FDA approval, maintained under unsanitary conditions At the... 

Press Release
2007-10-30 00:00:00
The U.S. Food and Drug Administration (FDA) has approved Tasigna (nilotinib... 

Press Release
2007-10-22 00:00:00
The U.S. Food and Drug Administration has approved Ixempra (ixabepilone), a... 

Press Release
2007-10-19 00:00:00
The U.S. Food and Drug Administration today approved a change in the storag... 

Press Release
2007-10-16 00:00:00
Raltegravir Tablets Used in Combination with Other Antiretroviral Agents ... 

Press Release
2007-10-04 00:00:00
The U.S. Food and Drug Administration today outlined a program aimed at inc... 

Press Release
2007-07-17 00:00:00
The U.S. Food and Drug Administration (FDA) approved for marketing the Pres... 

Global Regulatory .com values your privacy. For more information on our Privacy Policy, please visit Privacy Policy Please also visit Contract Laboratory.com,, Contract Clinical.com

DISCLAIMER: This information on Global Regulatory .com is provided as a service only. Company and product information is prepared by individual companies and has not been independently verified. As such Global RegulatoryInc can not be responsible for any loss or damage arising from the purchase, sale or use of any service or product through this site.

This site is owned and managed by Global Regulatory, Inc.