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    One of the biggest challenges facing health care providers today is enhancing safety and patient care while managing workflow efficiencies. As a division of the 13th largest global medical device manufacturer, B. Braun Medical Inc. (B.Braun) is uniquely poised to address this challenge. Guided by our Sharing Expertise® philosophy, B.Braun leads the way in developing infusion therapy and pain management products and services ...
    One of the biggest challenges facing health care providers today is enhancing safety and patient care while managing workflow efficiencies. As a division of the 13th largest global medical device manufacturer, B. Braun Medical Inc. (B.Braun) is uniquely poised to address this challenge. Guided by our Sharing Expertise® philosophy, B.Braun leads the way in developing infusion therapy and pain management products and services that meet the highest standards for quality, safety, sustainability and efficiency.

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    B. Braun MedicalUnited_States_of_America Flag
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    824 Twelfth Avenue Bethlehem, PA 18018-3524
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    INTERVIEW #SpeakPharma

    [Sponsored by another company]
    Alchem NicSelect™ grants customers royalty-free access to T-MAX™ tech for 3-in-1 vape satisfaction in flavour-restricted markets

    micAlchem NicSelect™ grants customers royalty-free access to T-MAX™ tech for 3-in-1 vape satisfaction in flavour-restricted markets

    With increasing flavour bans in key markets, vaping brands are facing significant challenges in providing satisfying alternatives to vapers and smokers looking to transition. Recognising this need, Alchem NicSelect™ is making a bold move by offering its key customers royalty-free and unrestricted geographical access to its revolutionary T-MAX™ technology.“At Alchem NicSelect™, we understand the urgency for vaping brands to adapt to new regulations without compromising on satisfaction. By offering royalty-free access to T-MAX™ technology, we empower our customers to provide the closest cigarette-like experience possible, even in markets with strict flavour restrictions,” said Riccardo Santambrogio, Europe Sales Manager.HIGHLIGHTS// offering royalty-free access to T-MAX™ technology/ unrestricted geographical access/ closest cigarette-like experience Addressing the biggest barrier: Nicotine satisfactionOne of the primary reasons many vapers are dissatisfied and smokers struggle to switch to vaping is that traditional nicotine solutions fail to replicate the rapid satisfaction provided by cigarettes. Nicotine replacement therapies (NRTs) and even conventional vaping products often lack the immediate nicotine hit, throat feel, and overall experience that smokers are accustomed to. T-MAX™ solves this problem by engineering a nicotine experience that closely mimics cigarette consumption without relying on flavours.T-MAX™ provides a unique 3-in-1 approach:1. The Speed of a Cigarette – Rapid nicotine delivery and rush within seconds for immediate satisfaction.2. The Power of Nicotine Salts – A stronger perceived nicotine effect without exceeding legal limits (20 mg/ml nicotine limit under the European Tobacco Products Directive). With T-MAX™, 8 mg/ml feels like 20 mg/ml, and 14 mg/ml feels like 40 mg/ml.3. The Throat Hit of Freebase Nicotine – Especially in a flavour-free formulation, the combined ingredients in T-MAX™ deliver an even more satisfying throat feel than expected from nicotine base, much closer to and more familiar with a cigarette throat feel that habitual smokers recognise.HIGHLIGHTS// unique 3-in-1 approach/ rush within seconds/ stronger perceived nicotine effect without exceeding legal limits/ more satisfying throat feel that habitual smokers recogniseNo flavour, but not less satisfyingWhile flavours have traditionally played a role in vaping adoption, market realities are shifting. With flavour bans spreading across regions, brands need solutions that deliver satisfaction without relying on taste. Consumer research has shown that T-MAX™ performs exceptionally well even without added flavours. Since most cigarette smokers do not smoke for the tobacco flavour but rather for the nicotine hit and habitual experience, T-MAX™ provides a viable alternative that aligns with new regulatory landscapes.HIGHLIGHTS// flavour bans spreading across regions/ T-MAX™ performs exceptionally well even without added flavoursEmpowering vape brands with free access to T-MAX™By granting customers royalty-free access to the T-MAX™ technology, Alchem NicSelect™ is removing barriers for vaping brands and original equipment manufacturers (OEMs) looking to adapt to regulatory changes. This open-access approach ensures that manufacturers can integrate T-MAX™ into their product lines without additional costs, allowing them to offer superior nicotine satisfaction in markets where flavours are no longer an option.HIGHLIGHTS// removing barriers for vaping brands and OEMs looking to adapt/ manufacturers can integrate T-MAX™ into product lines without additional costsThe future of vaping in restricted marketsWith T-MAX™, the vaping industry has a powerful tool to retain customers and convert smokers who have struggled with traditional vaping products. By delivering the key elements of cigarette satisfaction — without combustion or flavours — T-MAX™ is set to redefine what a satisfying vape experience means in a post-flavour-ban world.“Our commitment to innovation and accessibility means we are providing our customers with the solutions they need to navigate an evolving regulatory landscape. T-MAX™ allows brands to offer a highly satisfying experience that mimics smoking without relying on flavours. The message is clear: no flavour, but not less satisfying”, added Santambrogio.HIGHLIGHTS// powerful tool to retain customers and convert smokers/ delivering the key elements of cigarette satisfaction without combustion or flavours/ no flavour, but not less satisfying

    Impressions: 1241

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    06 May 2025
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    VLOG #PharmaReel

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    ReelPharmaProviding RSMs & API to Global Pharma CompaniesProviding RSMs & API to Global Pharma Companies

    Providing RSMs & API to Global Pharma Companies
    Providing RSMs & API to Global Pharma Companies

    reelProviding RSMs & API to Global Pharma Companies

    This PharmaReel showcases Allsino Pharmaceutical, a company that provides GMP-certified RSMs and APIs to global pharma companies, specializing in peptides, oligonucleotides, and small molecule CDMO services. Allsino has a presence in the US, EU, China and Japan.

    Impressions: 1278

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    DATA COMPILATION #PharmaFlow

    [Sponsored by another company]
    J&J’s Intra‑Cellular buyout, BMS’ oncology gambit, Sanofi’s Blueprint acquisition drive mega deals in H1 2025

    J&J’s Intra‑Cellular buyout, BMS’ oncology gambit, Sanofi’s Blueprint acquisition drive mega deals in H1 2025

    The pharmaceutical industry has witnessed a wave of mergers, acquisitions, and strategic partnerships so far in the first half (H1) of 2025, with deal values exceeding US$ 170 billion.PharmaCompass’ data shows oncology alone accounted for nearly US$ 47 billion in deal value, followed by US$ 18 billion each in immunology and psychiatry, US$ 17 billion in nutrition/weight loss and US$ 7 billion in neurology.Pharma majors such as Johnson & Johnson and Bristol Myers Squibb led with two deals worth over US$ 10 billion each. Sanofi executed a series of deals in the immunology and neuro-inflammation space. And Eli Lilly stood out for its aggressive dealmaking, which spanned oncology, pain, RNA therapies, and AI-driven oligonucleotides. In all, it signed seven deals worth over US$ 1 billion each. View Pharma & Biotech Acquisitions, Deals & Agreements in 2025 as of June 14 (Free Excel Available)H1 records several mega deals as J&J buys Intra-Cellular, BMS ties up with BioNTech, Sanofi acquires BlueprintJohnson & Johnson dominated headlines with its US$ 14.6 billion acquisition of Intra-Cellular Therapies in January 2025. This marks the largest biopharma deal since Novo Nordisk’s US$ 16.5 billion acquisition of Catalent in February 2024. This acquisition positions J&J as a formidable player in the neuroscience space. Bristol Myers Squibb entered into a US$ 11.1 billion partnership with BioNTech. The deal structure — US$ 3.5 billion in unconditional payments and up to US$ 7.6 billion in milestone payments — demonstrates BMS’ confidence in BNT327, a next-generation bispecific antibody in phase 3 trials for treating extensive stage small cell lung cancer and non-small cell lung cancer.Sanofi acquired Blueprint Medicines for US$ 9.5 billion in order to enhance its rare disease portfolio. The French drugmaker is also creating a comprehensive immunology portfolio. The company signed a US$ 1.9 billion deal for Dren Bio’s DR-0201 bispecific antibody for autoimmune diseases. Sanofi also acquired Vigil Neuroscience for US$ 470 million for its phase 2-ready Alzheimer’s disease candidate. Additionally, the drugmaker secured a US$ 1.84 billion global license agreement with Earendil Labs for two next-generation bispecific antibodies.Pfizer’s US$ 6.05 billion partnership with 3SBio provides it global licensing rights (excluding China) for SSGJ-707, a bispecific antibody currently undergoing multiple clinical trials in China for non-small cell lung cancer, metastatic colorectal cancer, and gynecological tumors. View Pharma & Biotech Acquisitions, Deals & Agreements in 2025 as of June 14 (Free Excel Available) Obesity gold rush sees Roche, AbbVie, Sciwind ink deals; Novo pledges over US$ 5 bn across three dealsThe obesity therapeutics market has triggered intense competition among pharmaceutical giants. Roche’s US$ 5.3 billion partnership with Zealand Pharma is focused on petrelintide, an amylin analog designed to preserve lean mass better than existing GLP-1-based treatments. The collaboration combines petrelintide with Roche’s dual GLP-1/GIP receptor agonist CT-388, creating a differentiated obesity treatment.Market leader Novo Nordisk has promised over US$ 5 billion across three major obesity deals in 2025. The US$ 2.2 billion Septerna collaboration targets oral small molecule medicines for obesity and cardiometabolic diseases.Novo signed a separate US$ 2 billion agreement with China’s United Biotechnology for UBT251, a triple agonist for GLP-1, GIP, and glucagon receptors in phase 2 clinical development for obesity, type 2 diabetes, and other diseases. The company’s third major deal, a US$ 1 billion partnership with Lexicon Pharmaceuticals, provides it access to LX9851, a molecule in preclinical development for obesity and associated metabolic disorders.Sciwind Biosciences secured a US$ 2.5 billion global licensing and collaboration agreement with Verdiva Bio Limited for the global development and commercialization of a portfolio of metabolic diseases therapies. AbbVie entered the amylin arena through its US$ 2.2 billion Gubra partnership for GUB014295, a candidate in phase 1 trials for treating obesity. View Pharma & Biotech Acquisitions, Deals & Agreements in 2025 as of June 14 (Free Excel Available) Molecular glue degraders draw investments; Lilly signs seven deals over US$ 1 billion eachMolecular glue degraders have emerged as a transformative therapeutic modality, attracting significant investment across multiple partnerships. AbbVie’s US$ 1.64 billion collaboration with Neomorph leverages the biotech’s leading molecular glue discovery platform for oncology and immunology applications.Genentech’s potential US$ 2.1 billion partnership with Orionis Biosciences focuses on small-molecule monovalent glue medicines for novel and challenging oncology targets. This is the second partnership between the two companies, following their initial 2023 collaboration.Eli Lilly has collaborated with Magnet Biomedicine, utilizing Magnet’s TrueGlue discovery platform for oncology applications. The deal could be worth up to US$ 1.3 billion.Eli Lilly has emerged as one of 2025’s most active dealmakers, with approximately seven deals exceeding US$ 1 billion each. The company’s US$ 2.5 billion Scorpion Therapeutics acquisition provides access to STX-478, an experimental oral therapy in early-stage trials for breast cancer and advanced solid tumors, potentially addressing 30 to 40 percent of hormone-positive breast cancer patients.On June 17, Lilly announced the acquisition of gene-editing startup Verve Therapeutics for US$ 1.3 billion. Lilly’s US$ 1 billion SiteOne acquisition announced in May brings STC-004, a phase 2-ready non-opioid chronic pain treatment to its pipeline. Other partnerships announced by Lilly include a US$ 1.4 billion capsid licensing deal with Sangamo for central nervous system disease genomic medicines and a US$ 1.3 billion collaboration with South Korean company Rznomics for RNA-based hearing loss treatments. Lilly has also strengthened its oligonucleotide pipeline through a potential US$ 1 billion collaboration with Creyon Bio for AI-designed oligonucleotide therapies targeting RNA. View Pharma & Biotech Acquisitions, Deals & Agreements in 2025 as of June 14 (Free Excel Available) Merck KGaA acquires SpringWorks for US$ 3.9 bn; Novartis buys out Anthos for US$ 3.1 bnAstraZeneca signed a US$ 5.3 billion AI-led research agreement with China’s CSPC Pharmaceuticals Group to advance the discovery of novel oral candidates for immunological diseases. Merck KGaA acquired SpringWorks for US$ 3.9 billion in April, which gave it access to two FDA-approved therapies — Ogsiveo (nirogacestat), the first and only approved therapy for adult patients with progressing desmoid tumors requiring systemic treatment, and Gomekli (mirdametinib), the first and only FDA-approved therapy for adults and children with neurofibromatosis type 1-associated plexiform neurofibromas.Novartis’ US$ 3.1 billion Anthos Therapeutics acquisition centered around abelacimab, a potential first-in-class monoclonal antibody currently in three phase 3 studies for stroke and systemic embolism prevention in atrial fibrillation patients.GSK’s US$ 2 billion acquisition of Boston Pharmaceuticals’ efimosfermin targets steatotic liver disease (fatty liver disease). The medicine is also in clinical development for MASH treatment. GSK’s second major deal involved the US$ 1.15 billion acquisition of US biotech IDRx, strengthening its gastrointestinal cancer portfolio.The pharma industry also drew some private equity interest as Bain Capital acquired Japan’s Mitsubishi Tanabe Pharma from Mitsubishi Chemical Group for US$ 3.3 billion. View Pharma & Biotech Acquisitions, Deals & Agreements in 2025 as of June 14 (Free Excel Available) Our viewDespite an uncertain geopolitical environment, the year has seen a surge in M&As and dealmaking in the first half of 2025. However, a sizable chunk of the acquisitions were bolt-on transactions, indicating that companies are not ready to take on risks, and are buying out smaller players who strategically fit into their operations. Going forward, there are indications that M&A activity will stay strong throughout 2025. 
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    Impressions: 2792

    https://www.pharmacompass.com/radio-compass-blog/j-j-s-intra-cellular-buyout-bms-oncology-gambit-sanofi-s-blueprint-acquisition-drive-mega-deals-in-h1-2025

    #PharmaFlow by PHARMACOMPASS
    19 Jun 2025
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    NEWS #PharmaBuzz

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    Enforcement Report - Week of April 16, 2025
    Enforcement Report - Week of April 16, 2025

    16 Apr 2025

    // FDA

    https://www.pharmacompass.com/pdf/news/enforcement-report-week-of-april-16-2025-39741.pdf

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    16 Apr 2025
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    FDA Approves Piperacillin-Tazobactam In Duplex By B Braun
    FDA Approves Piperacillin-Tazobactam In Duplex By B Braun

    10 Apr 2025

    // PR NEWSWIRE

    https://www.prnewswire.com/news-releases/b-braun-medical-inc-announces-us-fda-approval-of-piperacillin-and-tazobactam-for-injection-and-sodium-chloride-injection-in-the-duplex-drug-delivery-system-302423758.html

    PR NEWSWIRE
    10 Apr 2025
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    B. Braun Launches Cefazolin Pre-Mix in Duplex Containers
    B. Braun Launches Cefazolin Pre-Mix in Duplex Containers

    24 Mar 2025

    // PR NEWSWIRE

    https://www.prnewswire.com/news-releases/b-braun-launches-ready-to-activate-cefazolin-3-gram-pre-mix-in-duplex-containers-302409337.html

    PR NEWSWIRE
    24 Mar 2025
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    B. Braun, Baxter Recall Products Over Quality Concerns
    B. Braun, Baxter Recall Products Over Quality Concerns

    16 Aug 2024

    // FIERCE PHARMA

    https://www.fiercepharma.com/pharma/b-braun-baxter-launch-separate-recalls-over-particulate-concerns-and-excess-endotoxin-levels

    FIERCE PHARMA
    16 Aug 2024
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    B. Braun Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride for Injection
    B. Braun Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride for Injection

    08 Aug 2024

    // FDA

    https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/b-braun-issues-voluntary-nationwide-recall-09-sodium-chloride-injection-usp-1000-ml-e3-containers

    FDA
    08 Aug 2024
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    B Braun Interventional Systems introduces ACCEL All-Purpose
    B Braun Interventional Systems introduces ACCEL All-Purpose

    12 Jun 2024

    // PHARMABIZ

    https://www.pharmabiz.com/NewsDetails.aspx?aid=169699&sid=2

    PHARMABIZ
    12 Jun 2024
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    Drugs in Development

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    B. Braun Gains FDA Approval for DUPLEX Delivery of Piperacillin Combo

    Details:

    Piperacillin, a penicillin-class antibacterial, and Tazobactam, a beta-lactamase inhibitor, in the DUPLEX Drug Delivery System and Sodium Chloride, indicated for Intra-abdominal infections.


    Lead Product(s): Piperacillin Sodium,Tazobactam Sodium

    Therapeutic Area: Infections and Infectious Diseases Brand Name: Piperacillin and Tazobactam for Injection

    Study Phase: Approved FDFProduct Type: Antibiotic

    Sponsor: Inapplicable

    Deal Size: Inapplicable Upfront Cash: Inapplicable

    Deal Type: Inapplicable April 09, 2025

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    Lead Product(s) : Piperacillin Sodium,Tazobactam Sodium

    Therapeutic Area : Infections and Infectious Diseases

    Highest Development Status : Approved FDF

    Partner/Sponsor/Collaborator : Inapplicable

    Deal Size : Inapplicable

    Deal Type : Inapplicable

    DEALS_DEV arrow-down

    B. Braun Gains FDA Approval for DUPLEX Delivery of Piperacillin Combo

    Details : Piperacillin, a penicillin-class antibacterial, and Tazobactam, a beta-lactamase inhibitor, in the DUPLEX Drug Delivery System and Sodium Chloride, indicated for Intra-abdominal infections.

    Product Name : Piperacillin and Tazobactam for Injection

    Product Type : Antibiotic

    Upfront Cash : Inapplicable

    April 09, 2025

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    B. Braun Launches Ready-to-Activate Cefazolin 3 Gram Pre-Mix in DUPLEX® Containers

    Details:

    Cefazolin sodium is a bactericidal agent that acts by inhibition of bacterial cell wall synthesis. It is indicated for several infections, like respiratory, urinary infections in adult and pediatric.


    Lead Product(s): Cefazolin Sodium,Dextrose

    Therapeutic Area: Infections and Infectious Diseases Brand Name: Cefazolin Sodium Injection

    Study Phase: Approved FDFProduct Type: Antibiotic

    Sponsor: Inapplicable

    Deal Size: Inapplicable Upfront Cash: Inapplicable

    Deal Type: Inapplicable March 24, 2025

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    Lead Product(s) : Cefazolin Sodium,Dextrose

    Therapeutic Area : Infections and Infectious Diseases

    Highest Development Status : Approved FDF

    Partner/Sponsor/Collaborator : Inapplicable

    Deal Size : Inapplicable

    Deal Type : Inapplicable

    DEALS_DEV arrow-down

    B. Braun Launches Ready-to-Activate Cefazolin 3 Gram Pre-Mix in DUPLEX® Containers

    Details : Cefazolin sodium is a bactericidal agent that acts by inhibition of bacterial cell wall synthesis. It is indicated for several infections, like respiratory, urinary infections in adult and pediatric.

    Product Name : Cefazolin Sodium Injection

    Product Type : Antibiotic

    Upfront Cash : Inapplicable

    March 24, 2025

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    B. Braun Launches Levetiracetam in Sodium Chloride Injection Portfolio

    Details:

    Levetiracetam is indicated for adjunctive therapy in the treatment of Partial onset seizures in patients one month of age and older with epilepsy.


    Lead Product(s): Levetiracetam

    Therapeutic Area: Neurology Brand Name: Levetiracetam-Generic

    Study Phase: Approved FDFProduct Type: Other Small Molecule

    Sponsor: Inapplicable

    Deal Size: Inapplicable Upfront Cash: Inapplicable

    Deal Type: Inapplicable May 28, 2024

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    Lead Product(s) : Levetiracetam

    Therapeutic Area : Neurology

    Highest Development Status : Approved FDF

    Partner/Sponsor/Collaborator : Inapplicable

    Deal Size : Inapplicable

    Deal Type : Inapplicable

    DEALS_DEV arrow-down

    B. Braun Launches Levetiracetam in Sodium Chloride Injection Portfolio

    Details : Levetiracetam is indicated for adjunctive therapy in the treatment of Partial onset seizures in patients one month of age and older with epilepsy.

    Product Name : Levetiracetam-Generic

    Product Type : Other Small Molecule

    Upfront Cash : Inapplicable

    May 28, 2024

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    Healiva® Acquires Critical Cell Therapy Manufacturing Assets From B. Braun

    Details:

    The acquisition includes a qualified cell bank, which is essential for the GMP-compliant manufacturing of Healiva’s first cell therapy product, EpiDex®: an autologous epidermis derived from the patient’s own hair cells.


    Lead Product(s): Tissue-engineered Autologous Outer Root Sheath Keratinocyte

    Therapeutic Area: Trauma (Emergency, Injury, Surgery) Brand Name: Epidex

    Study Phase: Approved FDFProduct Type: Cell and Gene therapy

    Sponsor: Healiva

    Deal Size: Undisclosed Upfront Cash: Undisclosed

    Deal Type: Acquisition November 21, 2022

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    Lead Product(s) : Tissue-engineered Autologous Outer Root Sheath Keratinocyte

    Therapeutic Area : Trauma (Emergency, Injury, Surgery)

    Highest Development Status : Approved FDF

    Partner/Sponsor/Collaborator : Healiva

    Deal Size : Undisclosed

    Deal Type : Acquisition

    DEALS_DEV arrow-down

    Healiva® Acquires Critical Cell Therapy Manufacturing Assets From B. Braun

    Details : The acquisition includes a qualified cell bank, which is essential for the GMP-compliant manufacturing of Healiva’s first cell therapy product, EpiDex®: an autologous epidermis derived from the patient’s own hair cells.

    Product Name : Epidex

    Product Type : Cell and Gene therapy

    Upfront Cash : Undisclosed

    November 21, 2022

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    District Decision : Voluntary Action Indicated

    Inspection End Date : 2015-06-18

    B. Braun Medical

    City : Melsungen

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    Country/Area : DE

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    District : ORA

    Center : CDRH

    Project Area : Postmarket Assurance: Devices

    District Decision : Voluntary Action Indicated

    Inspection End Date : 2015-06-18

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    District Decision : Voluntary Action Indicated

    Inspection End Date : 2015-06-18

    B. Braun Medical

    City : Melsungen

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    Country/Area : DE

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    District : ORA

    Center : CDRH

    Project Area : Compliance: Devices

    District Decision : Voluntary Action Indicated

    Inspection End Date : 2015-06-18

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    District Decision : No Action Indicated

    Inspection End Date : 2015-02-19

    B. Braun Melsungen AG

    City : Melsungen

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    Country/Area : DE

    Zip :

    District : ORA

    Center : CDRH

    Project Area : Postmarket Assurance: Devices

    District Decision : No Action Indicated

    Inspection End Date : 2015-02-19

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    04

    FDA Audited

    USA
    Specialty & Agro Chemical
    Not Confirmed
    arrow

    FDA Audited

    USA
    arrow
    Specialty & Agro Chemical
    Not Confirmed

    District Decision : Voluntary Action Indicated

    Inspection End Date : 2015-02-19

    B. Braun Melsungen AG

    City : Melsungen

    State :

    Country/Area : DE

    Zip :

    District : ORA

    Center : CDRH

    Project Area : Compliance: Devices

    District Decision : Voluntary Action Indicated

    Inspection End Date : 2015-02-19

    blank

    Product
    Web Link

    Stock Recap
    #PipelineProspector

    Data Compilation
    #PharmaFlow

    05

    FDA Audited

    USA
    Specialty & Agro Chemical
    Not Confirmed
    arrow

    FDA Audited

    USA
    arrow
    Specialty & Agro Chemical
    Not Confirmed

    District Decision : No Action Indicated

    Inspection End Date : 2014-11-13

    B. Braun Medical

    City : Crissier

    State :

    Country/Area : CH

    Zip :

    District : ORA

    Center : CDER

    Project Area : Drug Quality Assurance

    District Decision : No Action Indicated

    Inspection End Date : 2014-11-13

    blank

    Product
    Web Link

    Stock Recap
    #PipelineProspector

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    06

    FDA Audited

    USA
    Specialty & Agro Chemical
    Not Confirmed
    arrow

    FDA Audited

    USA
    arrow
    Specialty & Agro Chemical
    Not Confirmed

    District Decision : No Action Indicated

    Inspection End Date : 2014-06-03

    B. Braun Medical

    City : Sempach

    State :

    Country/Area : CH

    Zip :

    District : ORA

    Center : CDRH

    Project Area : Compliance: Devices

    District Decision : No Action Indicated

    Inspection End Date : 2014-06-03

    blank

    Product
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    07

    FDA Audited

    USA
    Specialty & Agro Chemical
    Not Confirmed
    arrow

    FDA Audited

    USA
    arrow
    Specialty & Agro Chemical
    Not Confirmed

    District Decision : No Action Indicated

    Inspection End Date : 2014-05-20

    B. Braun Melsungen AG

    City : Melsungen

    State :

    Country/Area : DE

    Zip :

    District : ORA

    Center : CDER

    Project Area : Drug Quality Assurance

    District Decision : No Action Indicated

    Inspection End Date : 2014-05-20

    blank

    Product
    Web Link

    Stock Recap
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    08

    FDA Audited

    USA
    Specialty & Agro Chemical
    Not Confirmed
    arrow

    FDA Audited

    USA
    arrow
    Specialty & Agro Chemical
    Not Confirmed

    District Decision : Voluntary Action Indicated

    Inspection End Date : 2014-04-10

    B. Braun Medical

    City : Tochigitochigi

    State :

    Country/Area : JP

    Zip :

    District : ORA

    Center : CDRH

    Project Area : Compliance: Devices

    District Decision : Voluntary Action Indicated

    Inspection End Date : 2014-04-10

    blank

    Product
    Web Link

    Stock Recap
    #PipelineProspector

    Data Compilation
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    09

    FDA Audited

    USA
    Specialty & Agro Chemical
    Not Confirmed
    arrow

    FDA Audited

    USA
    arrow
    Specialty & Agro Chemical
    Not Confirmed

    District Decision : Voluntary Action Indicated

    Inspection End Date : 2014-03-20

    B. Braun Medical

    City : Rubi

    State :

    Country/Area : ES

    Zip :

    District : ORA

    Center : CDRH

    Project Area : Compliance: Devices

    District Decision : Voluntary Action Indicated

    Inspection End Date : 2014-03-20

    blank

    Product
    Web Link

    Stock Recap
    #PipelineProspector

    Data Compilation
    #PharmaFlow

    10

    FDA Audited

    USA
    Specialty & Agro Chemical
    Not Confirmed
    arrow

    FDA Audited

    USA
    arrow
    Specialty & Agro Chemical
    Not Confirmed

    District Decision : Voluntary Action Indicated

    Inspection End Date : 2014-02-13

    B. Braun Medical

    City : Irvine

    State : CA

    Country/Area : US

    Zip : 92614

    District : LOS

    Center : CDER

    Project Area : Drug Quality Assurance

    District Decision : Voluntary Action Indicated

    Inspection End Date : 2014-02-13

    blank

    Product
    Web Link

    Stock Recap
    #PipelineProspector

    Data Compilation
    #PharmaFlow

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