04 Oct 2024
// PRESS RELEASE
17 Jun 2024
// PRESS RELEASE
13 Jun 2024
// PRESS RELEASE
Latest Content by PharmaCompass
Ethypharm is an international Pharma company with European roots manufacturing and commercializing essential drugs all over the world.
About
CPhI India 2024CPhI India 2024
Industry Trade Show
Not Confirmed
26-28 November, 2024
CPhI WW FrankfurtCPhI WW Frankfurt
Industry Trade Show
Booth #5.0D100
28-30 October, 2025
American Pharma SummitAmerican Pharma Summit
Industry Trade Show
Not Confirmed
18-19 November, 2024
CONTACT DETAILS
Events
Webinars & Exhibitions
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CPhI India 2024CPhI India 2024
Industry Trade Show
Not Confirmed
26-28 November, 2024
CPhI WW FrankfurtCPhI WW Frankfurt
Industry Trade Show
Booth #5.0D100
28-30 October, 2025
American Pharma SummitAmerican Pharma Summit
Industry Trade Show
Not Confirmed
18-19 November, 2024
CORPORATE CONTENT #SupplierSpotlight
04 Oct 2024
// PRESS RELEASE
https://www.ethypharm.com/blog/newsroom/ethypharm-announces-the-appointment-of-eric-chevalier-as-group-human-resources-director/
17 Jun 2024
// PRESS RELEASE
https://www.ethypharm.com/wp-content/uploads/2024/06/18-06-24-Press-Release-Argatroban-Ethypharm-Final.pdf
13 Jun 2024
// PRESS RELEASE
https://www.ethypharm.com/wp-content/uploads/2024/06/13062024_Group-PR_-Ethypharm-Expands-its-Mesalazine-Portfolio-in-China_FINAL-PR-NEWSWIRE.pdf
06 Apr 2024
// PRESS RELEASE
https://www.ethypharm.com/wp-content/uploads/2022/10/Agreement-Gaia-AG-EN.pdf
13 Jun 2023
// PRESS RELEASE
https://www.ethypharm.com/wp-content/uploads/2023/06/PR-Xavier-LASSERRE-appointed_CCO_Ethypharm-final.pdf
01 May 2023
// PRESS RELEASE
https://www.ethypharm.com/wp-content/uploads/2023/05/Aurora_Ethypharm_Extension-Pilot-Program_FINAL-1.pdf
Registrant Name : Samchundang Pharmaceutical Co., Ltd.
Registration Date : 2015-05-20
Registration Number : 20131031-127-H-243-13(1)
Manufacturer Name : Ethypharm@[Starting material '...
Manufacturer Address : Zone industrielle de Saint-Arunoult 28 170 Chateauneuf-en-Thymerais, France@Old Madra...
Registrant Name : Wooshin Labotech Co., Ltd.
Registration Date : 2013-10-31
Registration Number : 20131031-127-H-243-13
Manufacturer Name : Ethypharm@[Starting material '...
Manufacturer Address : Zone industrielle de Saint-Arunoult 28 170 Chateauneuf-en-Thymerais, France@Old Madra...
Registrant Name : Wooshin Labotech Co., Ltd.
Registration Date : 2021-05-25
Registration Number : 20210525-209-J-725
Manufacturer Name : Shanghai Ethypharm Pharmaceuti...
Manufacturer Address : No.278, Qianyun Road, South Of No.16 Bridge, State Road 318, Xujing, Qingpu District,...
Registrant Name : Wooshin Labotech Co., Ltd.
Registration Date : 2021-05-25
Registration Number : 20210525-209-J-726
Manufacturer Name : Shanghai Ethypharm Pharmaceuti...
Manufacturer Address : No.278, Qianyun Road, South Of No.16 Bridge, State Road 318, Xujing, Qingpu District,...
Registrant Name : Kukjeon Pharmaceutical Co., Ltd.
Registration Date : 2021-10-07
Registration Number : 20210525-209-J-725(1)
Manufacturer Name : Shanghai Ethypharm Pharmaceuti...
Manufacturer Address : No.278, Qianyun Road, South of No,16 Bridge, State Road 318, Xujing, Qingpu District,...
Registrant Name : Samchundang Pharmaceutical Co., Ltd.
Registration Date : 2021-09-24
Registration Number : 20210525-209-J-726(1)
Manufacturer Name : Shanghai Ethypharm Pharmaceuti...
Manufacturer Address : No.278, Qianyun Road, South of No,16 Bridge, State Road 318, Xujing, Qingpu District,...
Details:
Ethypharm acquired Mitsubishi Tanabe's selective antithrombin agent Arganova (argatroban monohydrate) in Europe. It is indicated for the treatment of heparin-induced thrombocytopenia type II.
Lead Product(s): Argatroban Monohydrate
Therapeutic Area: Hematology Brand Name: Arganova
Study Phase: ApprovedProduct Type: Small molecule
Recipient: Mitsubishi Tanabe Pharma
Deal Size: Undisclosed Upfront Cash: Undisclosed
Deal Type: Acquisition June 17, 2024
Lead Product(s) : Argatroban Monohydrate
Therapeutic Area : Hematology
Highest Development Status : Approved
Recipient : Mitsubishi Tanabe Pharma
Deal Size : Undisclosed
Deal Type : Acquisition
Acquisition of Argatroban Business in Europe
Details : Ethypharm acquired Mitsubishi Tanabe's selective antithrombin agent Arganova (argatroban monohydrate) in Europe. It is indicated for the treatment of heparin-induced thrombocytopenia type II.
Brand Name : Arganova
Molecule Type : Small molecule
Upfront Cash : Undisclosed
June 17, 2024
Details:
The acquisition will enable Ethypharm a full portfolio of Mesalazine forms, including a suppository form of Etiasa (mesalazine), used to treat IBD such as ulcerative colitis and Crohn's disease.
Lead Product(s): Mesalazine
Therapeutic Area: Gastroenterology Brand Name: Etiasa
Study Phase: ApprovedProduct Type: Small molecule
Recipient: Anbison
Deal Size: Undisclosed Upfront Cash: Undisclosed
Deal Type: Acquisition June 13, 2024
Lead Product(s) : Mesalazine
Therapeutic Area : Gastroenterology
Highest Development Status : Approved
Recipient : Anbison
Deal Size : Undisclosed
Deal Type : Acquisition
Ethypharm expands its Mesalazine (Etiasa®) Portfolio in China
Details : The acquisition will enable Ethypharm a full portfolio of Mesalazine forms, including a suppository form of Etiasa (mesalazine), used to treat IBD such as ulcerative colitis and Crohn's disease.
Brand Name : Etiasa
Molecule Type : Small molecule
Upfront Cash : Undisclosed
June 13, 2024
Details:
Company received marketing authorisations (MA) for the 1st Immediate-Release orodispersible tablets of morphine, an opioid receptor agonist for the management of severe pain.
Lead Product(s): Morphine Sulfate
Therapeutic Area: Neurology Brand Name: Undisclosed
Study Phase: ApprovedProduct Type: Small molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable December 02, 2021
Lead Product(s) : Morphine Sulfate
Therapeutic Area : Neurology
Highest Development Status : Approved
Partner/Sponsor/Collaborator : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
Ethypharm Gains EU Approval for Morphine Immediate Release Tablets
Details : Company received marketing authorisations (MA) for the 1st Immediate-Release orodispersible tablets of morphine, an opioid receptor agonist for the management of severe pain.
Brand Name : Undisclosed
Molecule Type : Small molecule
Upfront Cash : Not Applicable
December 02, 2021
Details:
Ethypharm has acquired the exclusive rights for the development, registration and commercialization in the top 5 European markets of a novel celecoxib formulation already approved in the US for the acute treatment of migraine. Celecoxib is developed by Dr Reddy's.
Lead Product(s): Celecoxib
Therapeutic Area: Neurology Brand Name: Elyxyb
Study Phase: ApprovedProduct Type: Small molecule
Recipient: Dr. Reddy\'s Laboratories
Deal Size: Undisclosed Upfront Cash: Undisclosed
Deal Type: Acquisition May 19, 2021
Lead Product(s) : Celecoxib
Therapeutic Area : Neurology
Highest Development Status : Approved
Recipient : Dr. Reddy\'s Laboratories
Deal Size : Undisclosed
Deal Type : Acquisition
Ethypharm Reinforces its Late-Stage R&D Pipeline with a Novel Acute Treatment of Migraine
Details : Ethypharm has acquired the exclusive rights for the development, registration and commercialization in the top 5 European markets of a novel celecoxib formulation already approved in the US for the acute treatment of migraine. Celecoxib is developed by D...
Brand Name : Elyxyb
Molecule Type : Small molecule
Upfront Cash : Undisclosed
May 19, 2021
Details:
Orphelia has granted Ethypharm exclusive rights under a license agreement to commercialize Kigabeq (vigabatrin) in China. Kigabeq is indicated as a first-line treatment for infantile spasms.
Lead Product(s): Vigabatrin
Therapeutic Area: Neurology Brand Name: Kigabeq
Study Phase: ApprovedProduct Type: Small molecule
Recipient: Orphelia Pharma
Deal Size: Undisclosed Upfront Cash: Undisclosed
Deal Type: Licensing Agreement January 19, 2021
Lead Product(s) : Vigabatrin
Therapeutic Area : Neurology
Highest Development Status : Approved
Recipient : Orphelia Pharma
Deal Size : Undisclosed
Deal Type : Licensing Agreement
ORPHELIA, Ethypharm Sign Kigabeq® Licensing Deal for China
Details : Orphelia has granted Ethypharm exclusive rights under a license agreement to commercialize Kigabeq (vigabatrin) in China. Kigabeq is indicated as a first-line treatment for infantile spasms.
Brand Name : Kigabeq
Molecule Type : Small molecule
Upfront Cash : Undisclosed
January 19, 2021
Details:
Triamcinolone Hexacetonide is a longest-acting corticosteroid for intra articular injection. The companies have agreed to a small upfront fee along with milestone payments at the time of FDA approval, at commercial product launch, and upon certain sales milestones.
Lead Product(s): Triamcinolone Acetonide
Therapeutic Area: Immunology Brand Name: Undisclosed
Study Phase: ApprovedProduct Type: Small molecule
Sponsor: Medexus Pharmaceuticals
Deal Size: Undisclosed Upfront Cash: Undisclosed
Deal Type: Licensing Agreement December 18, 2020
Lead Product(s) : Triamcinolone Acetonide
Therapeutic Area : Immunology
Highest Development Status : Approved
Partner/Sponsor/Collaborator : Medexus Pharmaceuticals
Deal Size : Undisclosed
Deal Type : Licensing Agreement
Details : Triamcinolone Hexacetonide is a longest-acting corticosteroid for intra articular injection. The companies have agreed to a small upfront fee along with milestone payments at the time of FDA approval, at commercial product launch, and upon certain sales ...
Brand Name : Undisclosed
Molecule Type : Small molecule
Upfront Cash : Undisclosed
December 18, 2020
Details:
Under the agreement, CTRS has granted Ethypharm exclusive rights to distribute Orphacol (cholic acid) in China. It is indicated for the two rare inborn errors of primary bile acid synthesis.
Lead Product(s): Cholic Acid
Therapeutic Area: Genetic Disease Brand Name: Orphacol
Study Phase: ApprovedProduct Type: Small molecule
Recipient: Laboratoires CTRS
Deal Size: Undisclosed Upfront Cash: Undisclosed
Deal Type: Agreement November 10, 2020
Lead Product(s) : Cholic Acid
Therapeutic Area : Genetic Disease
Highest Development Status : Approved
Recipient : Laboratoires CTRS
Deal Size : Undisclosed
Deal Type : Agreement
Ethypharm, CTRS Partner to Register Orphacol® in China
Details : Under the agreement, CTRS has granted Ethypharm exclusive rights to distribute Orphacol (cholic acid) in China. It is indicated for the two rare inborn errors of primary bile acid synthesis.
Brand Name : Orphacol
Molecule Type : Small molecule
Upfront Cash : Undisclosed
November 10, 2020
Details:
The collaboration is intended to accelerate the manufacture and batch release of fentanyl injection; one of the critical medicines needed for the treatment of COVID-19 patients.
Lead Product(s): Fentanyl
Therapeutic Area: Infections and Infectious Diseases Brand Name: Undisclosed
Study Phase: UndisclosedProduct Type: Small molecule
Recipient: Reading Scientific Services
Deal Size: Undisclosed Upfront Cash: Undisclosed
Deal Type: Partnership June 04, 2020
Lead Product(s) : Fentanyl
Therapeutic Area : Infections and Infectious Diseases
Highest Development Status : Undisclosed
Recipient : Reading Scientific Services
Deal Size : Undisclosed
Deal Type : Partnership
Ethypharm and RSSL Fast-Track Medicine for COVID-19 Patients
Details : The collaboration is intended to accelerate the manufacture and batch release of fentanyl injection; one of the critical medicines needed for the treatment of COVID-19 patients.
Brand Name : Undisclosed
Molecule Type : Small molecule
Upfront Cash : Undisclosed
June 04, 2020
Regulatory Info :
Registration Country : France
Dosage Form : Ampoule
Brand Name :
Dosage Strength : 200MG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Dosage Form : Vial
Brand Name :
Dosage Strength : 250MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : Norway
Dosage Form : Solution for injection
Brand Name : Adrenalin Martindale Phar...
Dosage Strength : 0.1mg/ml
Packaging : Ampoule av glass 10 10ml
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Dosage Form : Solution for injection
Brand Name : Adrenalin Ethypharm
Dosage Strength : 1mg/ml
Packaging : Ampoule av glass 10 1ml
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : France
Dosage Form : Powder for Solution for ...
Brand Name :
Dosage Strength : 20MCG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Dosage Form : Capsule
Brand Name :
Dosage Strength : 125MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Dosage Form : Capsule
Brand Name :
Dosage Strength : 80MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Dosage Form : Ampoule
Brand Name :
Dosage Strength : 6.75MG/0.9ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Dosage Form : Vial
Brand Name :
Dosage Strength : 37.5MG/5ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Dosage Form : Ampoule
Brand Name :
Dosage Strength : 1MG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
RLD : No
TE Code : AB
Dosage Form : TABLET; SUBLINGUAL
Proprietary Name : BUPRENORPHINE HYDROCHLOR...
Dosage Strength : EQ 2MG BASE
Approval Date : 2010-09-24
Application Number : 90622
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; SUBLINGUAL
Proprietary Name : BUPRENORPHINE HYDROCHLOR...
Dosage Strength : EQ 8MG BASE
Approval Date : 2010-09-24
Application Number : 90622
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Dosage Form : TABLET; SUBLINGUAL
Proprietary Name : BUPRENORPHINE HYDROCHLOR...
Dosage Strength : EQ 2MG BASE;EQ 0.5MG BAS...
Approval Date : 2015-10-16
Application Number : 204431
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Dosage Form : TABLET; SUBLINGUAL
Proprietary Name : BUPRENORPHINE HYDROCHLOR...
Dosage Strength : EQ 8MG BASE;EQ 2MG BASE
Approval Date : 2015-10-16
Application Number : 204431
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : CAPSULE, DELAYED REL PELLETS; ...
Proprietary Name : ESOMEPRAZOLE MAGNESIUM
Dosage Strength : EQ 20MG BASE
Approval Date : 2021-03-31
Application Number : 90841
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : CAPSULE, DELAYED REL PELLETS; ...
Proprietary Name : ESOMEPRAZOLE MAGNESIUM
Dosage Strength : EQ 40MG BASE
Approval Date : 2021-03-31
Application Number : 90841
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
Regulatory Info :
Registration Country : Norway
Dosage Form : Solution for injection
Dosage Strength : 0.1mg/ml
Packaging : Ampoule av glass ...
Brand Name : Adrenalin Martindale Pharma
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Dosage Form : Solution for injection
Dosage Strength : 1mg/ml
Packaging : Ampoule av glass ...
Brand Name : Adrenalin Ethypharm
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Dosage Form : Lyofilisattablett
Dosage Strength : 8 mg
Packaging : Endose blister pa...
Brand Name : Espranor
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Dosage Form : Lyofilisattablett
Dosage Strength : 2 mg
Packaging : Endose blister pa...
Brand Name : Espranor
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Italy
Dosage Form : Extended Release Hard Capsules
Dosage Strength : 10 mg
Packaging : 16 UNITS 10 MG - O...
Brand Name : TWICE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Dosage Form : Extended Release Hard Capsules
Dosage Strength : 100 mg
Packaging : 16 UNITS 100 MG - ...
Brand Name : TWICE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Dosage Form : Extended Release Hard Capsules
Dosage Strength : 30 mg
Packaging : 16 UNITS 30 MG - O...
Brand Name : TWICE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Dosage Form : Extended Release Hard Capsules
Dosage Strength : 60 mg
Packaging : 16 UNITS 60 MG - O...
Brand Name : TWICE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Dosage Form : CAPSULE (EXTENDED RELEASE)
Dosage Strength : 15MG
Packaging : 20/50
Brand Name : M-ESLON
Approval Date :
Application Number : 2177749
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Dosage Form : CAPSULE (EXTENDED RELEASE)
Dosage Strength : 200MG
Packaging : 20/50
Brand Name : M-ESLON
Approval Date :
Application Number : 2177757
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Dosage Form : CAPSULE (EXTENDED RELEASE)
Dosage Strength : 30MG
Packaging : 20/50
Brand Name : M-ESLON
Approval Date :
Application Number : 2019949
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Dosage Form : CAPSULE (EXTENDED RELEASE)
Dosage Strength : 100MG
Packaging : 20/50
Brand Name : M-ESLON
Approval Date :
Application Number : 2019965
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Dosage Form : CAPSULE (EXTENDED RELEASE)
Dosage Strength : 60MG
Packaging : 20/50
Brand Name : M-ESLON
Approval Date :
Application Number : 2019957
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Dosage Form : CAPSULE (EXTENDED RELEASE)
Dosage Strength : 10MG
Packaging : 20/50
Brand Name : M-ESLON
Approval Date :
Application Number : 2019930
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Regulatory Info :
Registration Country : France
Dosage Form : Ampoule
Brand Name :
Dosage Strength : 200MG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Dosage Form : Vial
Brand Name :
Dosage Strength : 250MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Dosage Form : Powder for Solution for Infu...
Brand Name :
Dosage Strength : 20MCG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Dosage Form : Capsule
Brand Name :
Dosage Strength : 80MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Dosage Form : Capsule
Brand Name :
Dosage Strength : 125MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Dosage Form : Vial
Brand Name :
Dosage Strength : 37.5MG/5ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Dosage Form : Ampoule
Brand Name :
Dosage Strength : 6.75MG/0.9ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Dosage Form : Ampoule
Brand Name :
Dosage Strength : 600MCG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Dosage Form : Ampoule
Brand Name :
Dosage Strength : 1MG/ML
Packaging :
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Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Dosage Form : Vial
Brand Name :
Dosage Strength : 500MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Services
Packaging
Drug Product Manufacturing
Pharma Service : Drug Product Manufacturing
Category : Liquid
Sub Category : Controlled Substance
Pharma Service : Drug Product Manufacturing
Pharma Service : Drug Product Manufacturing
Category : Suspension
Sub Category : Injectable
Pharma Service : Drug Product Manufacturing
Pharma Service : Drug Product Manufacturing
Category : Lyophilization
Sub Category : Overview
Pharma Service : Drug Product Manufacturing
Pharma Service : Drug Product Manufacturing
Category : Granule / Pellet
Sub Category : Modified Release
Pharma Service : Drug Product Manufacturing
Pharma Service : Drug Product Manufacturing
Category : Solution
Sub Category : Injectable
Pharma Service : Drug Product Manufacturing
Pharma Service : Drug Product Manufacturing
Pharma Service : Drug Product Manufacturing
Pharma Service : Drug Product Manufacturing
Category : Injectable / Parenteral
Sub Category : Overview
Pharma Service : Drug Product Manufacturing
Pharma Service : Drug Product Manufacturing
Category : Injectable / Parenteral
Sub Category : Pre-Filled Syringe
Pharma Service : Drug Product Manufacturing
Pharma Service : Drug Product Manufacturing
Pharma Service : Drug Product Manufacturing
Pharma Service : Drug Product Manufacturing
Category : Capsule
Sub Category : Controlled Substance
Pharma Service : Drug Product Manufacturing
Pharma Service : Drug Product Manufacturing
Category : Capsule
Sub Category : High Potency APIs (HPAPIs)
Pharma Service : Drug Product Manufacturing
Pharma Service : Drug Product Manufacturing
Category : Capsule
Sub Category : Controlled / Immediate / Modified Release
Pharma Service : Drug Product Manufacturing
Pharma Service : Drug Product Manufacturing
Category : Capsule
Sub Category : Hard Capsule
Pharma Service : Drug Product Manufacturing
Pharma Service : Drug Product Manufacturing
Pharma Service : Drug Product Manufacturing
Pharma Service : Drug Product Manufacturing
Category : Tablet
Sub Category : Controlled Substance
Pharma Service : Drug Product Manufacturing
Pharma Service : Drug Product Manufacturing
Category : Tablet
Sub Category : High Potency APIs (HPAPIs)
Pharma Service : Drug Product Manufacturing
Pharma Service : Drug Product Manufacturing
Category : Tablet
Sub Category : Controlled / Immediate / Modified Release
Pharma Service : Drug Product Manufacturing
Pharma Service : Drug Product Manufacturing
Category : Tablet
Sub Category : Sustained Release
Pharma Service : Drug Product Manufacturing
Pharma Service : Drug Product Manufacturing
Pharma Service : Drug Product Manufacturing
API & Drug Product Development
Pharma Service : API & Drug Product Development
Category : Formulation Development
Sub Category : Injectable / Parenteral
Pharma Service : API & Drug Product Development
Pharma Service : API & Drug Product Development
Category : Formulation Development
Sub Category : Sterile Liquid Formulation
Pharma Service : API & Drug Product Development
Pharma Service : API & Drug Product Development
Category : Formulation Development
Sub Category : Lyophilization
Pharma Service : API & Drug Product Development
Pharma Service : API & Drug Product Development
Category : Formulation Development
Sub Category : Tablet
Pharma Service : API & Drug Product Development
Pharma Service : API & Drug Product Development
Category : Formulation Development
Sub Category : Capsule
Pharma Service : API & Drug Product Development
Pharma Service : API & Drug Product Development
Category : Formulation Development
Sub Category : Liquid Formulation
Pharma Service : API & Drug Product Development
Pharma Service : API & Drug Product Development
Category : Formulation Development
Sub Category : Controlled / Immediate / Modified Release
Pharma Service : API & Drug Product Development
Pharma Service : API & Drug Product Development
Category : Formulation Development
Sub Category : Controlled Substance
Pharma Service : API & Drug Product Development
Inspections and registrations
District Decision : Voluntary Action Indicated
Inspection End Date : 2020-11-05
City : Le Grand Quevilly CEDEX
State :
Country/Area : France
Zip :
District :
Center :
Project Area : Drug Quality Assurance
District Decision : Voluntary Action Indicated
Inspection End Date : 2020-11-05
District Decision : Voluntary Action Indicated
Inspection End Date : 2009-02-23
City : Chateauneuf En Thymerais
State :
Country/Area : France
Zip :
District :
Center :
Project Area : Drug Quality Assurance
District Decision : Voluntary Action Indicated
Inspection End Date : 2009-02-23
District Decision : Voluntary Action Indicated
Inspection End Date : 2012-09-13
City : Chateauneuf En Thymerais
State :
Country/Area : France
Zip :
District :
Center :
Project Area : Drug Quality Assurance
District Decision : Voluntary Action Indicated
Inspection End Date : 2012-09-13
District Decision : No Action Indicated
Inspection End Date : 2014-12-12
City : Chateauneuf En Thymerais
State :
Country/Area : France
Zip :
District :
Center :
Project Area : Drug Quality Assurance
District Decision : No Action Indicated
Inspection End Date : 2014-12-12
District Decision : Voluntary Action Indicated
Inspection End Date : 2018-02-22
City : Chateauneuf En Thymerais
State :
Country/Area : France
Zip :
District :
Center :
Project Area : Drug Quality Assurance
District Decision : Voluntary Action Indicated
Inspection End Date : 2018-02-22
District Decision : Voluntary Action Indicated
Inspection End Date : 2023-03-25
City : Chateauneuf En Thymerais
State :
Country/Area : France
Zip :
District :
Center :
Project Area : Drug Quality Assurance
District Decision : Voluntary Action Indicated
Inspection End Date : 2023-03-25
District Decision : Voluntary Action Indicated
Inspection End Date : 2009-02-19
City : Le Grand Quevilly CEDEX
State :
Country/Area : France
Zip :
District :
Center :
Project Area : Drug Quality Assurance
District Decision : Voluntary Action Indicated
Inspection End Date : 2009-02-19
District Decision : Voluntary Action Indicated
Inspection End Date : 2012-10-19
City : Le Grand Quevilly CEDEX
State :
Country/Area : France
Zip :
District :
Center :
Project Area : Drug Quality Assurance
District Decision : Voluntary Action Indicated
Inspection End Date : 2012-10-19
District Decision : No Action Indicated
Inspection End Date : 2014-12-05
City : Le Grand Quevilly CEDEX
State :
Country/Area : France
Zip :
District :
Center :
Project Area : Drug Quality Assurance
District Decision : No Action Indicated
Inspection End Date : 2014-12-05
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