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  1. Active Pharmaceutical Ingredient Contract Manufacturing Company

    GMP Pharmaceutical and Biologic contract manufacturing company BioVectra Inc. is a FDA compliant pharmaceutical and biologic contract manufacturing company ...
    quality assurance2
    fermentation1
    paclitaxel1
    PEGylation1
    drug master file1
    FDA compliant1
    microbial fermentation1
    docetaxel1
    taxanes1
    FDA regulatory compliance1
    plant extraction1
    animal extraction1
    GMP contract manufacturing1
    adenosine deaminase ADA0
    Animal free IPTG0
    biologic fermentation0
    cholesterol esterase0
    contract API manufacturing0
    contract biologic manufacturer0
    cytotoxic API0
    cytotoxic fermentation0
    cytotoxic manufacturing0
    Dithioerythritol DTE0
    dithiothreitol DTT0
    downstream processing DSP0
    ICH Q7 guidelines0
    MPEG reagents0
    natural product extraction0
    PEG reagents0
    pharmaceutical fermentation0
    polyethylene glycol reagents0

    www.biovectra.com - 2009-02-06

  2. DNA Life Sciences, Providing GMP Compliance consultation, regulatory and technical expertise to manufacturers of Drug Products, Active Pharmaceutical ...

    Providing GMP Compliance consultation, regulatory and technical expertise to manufacturers of Drug Products, Active Pharmaceutical Ingredients, and Medical ...
    Pharmaceutical3
    Active2
    Ingredients2
    GMP2
    Regulatory Compliance2
    CGMP1
    Quality Systems1
    Process Validation1
    Cleaning Validation1
    Clinical Supplies1
    GMP Training1
    GMP Compliance1
    Drug Master File1
    Clinical Trial Materials1
    GMP Consultant1
    Warning Letters1
    FDA Regulatory Consultant1
    Q7A1
    Pre-approval Inspections1
    API and GMP1

    dna-india.net - 2009-04-11

  3. GMP Compliance Consultation for Pharmaceutical Industries Worldwide

    Providing GMP Compliance consultation, regulatory and technical expertise to manufacturers of Drug Products, Active Pharmaceutical Ingredients, and Medical ...
    Pharmaceutical3
    Active2
    Ingredients2
    GMP2
    Regulatory Compliance2
    CGMP1
    Quality Systems1
    Process Validation1
    Cleaning Validation1
    Clinical Supplies1
    GMP Training1
    GMP Compliance1
    Drug Master File1
    Clinical Trial Materials1
    GMP Consultant1
    Warning Letters1
    FDA Regulatory Consultant1
    Q7A1
    Pre-approval Inspections1
    API and GMP1

    www.harpazconsulting.com - 2009-02-13

  4. News from FeF Chemicals and welcome by the Managing Director

    FeF Chemicals A/S is the partner of choice when it comes to quaternary ammonium compounds (Quats).
    cosmetic3
    Pharmaceutical3
    chemical3
    API2
    CEP2
    COS1
    USP1
    cGMP1
    DMF1
    fine chemical1
    Drug Master File1
    Certificate of Suitability1
    quaternary ammonium compounds1
    Ph.Eur.1
    quats - FeF Chemicals1

    www.fef-chem.com - 2009-02-06

  5. Mandava Associates

    Clinical Research Organization, Scientific Regulatory Consultants - new drugs, medical devices, antimicrobial products; agriculture, household, industrial and ...
    Drugs3
    Chemicals2
    Cleaners2
    Devices2
    Diagnostics2
    EPA2
    CRO2
    Clinical trials2
    Crop Protection1
    Antibacterial1
    Antimicrobial1
    Detergents1
    ANDA1
    Disinfectants1
    Degreasing1
    Biocide1
    Biochemicals1
    DMF1
    Agricultural chemicals1
    510 k1
    510k1
    Department of Agriculture1
    Environmental Toxicology1
    Drug Master File1
    Environmental Fate1
    Federal Registration1
    Agricultural pesticides1
    Biochemical Pest Control0
    Device Master File0
    Direct Food Additives0
    FD&C Act0

    www.mandava.com - 2009-02-03

  6. Glenmark Pharmaceuticals Ltd.

    Research driven Global integrated Pharmaceutical Company
    Diabetes3
    Drugs3
    Brazil3
    Forest2
    Asthma2
    GPL2
    Dermatology2
    Cardiology2
    Candid2
    ENT2
    COPD1
    Drug Discovery1
    Financial information1
    Family Physician1
    Diabetics1
    ANDA1
    General Practitioner1
    DMF1
    Basic research1
    ANVISA1
    Drug Master File1
    Drug Delivery System1
    Diabetes Type II1
    Glenmark1
    Forest Laboratories1
    Ascoril1
    Formulation exports1
    Gold standard molecule1
    Gracewell1
    GRC 38861
    GRC 82001

    glenmarkpharma.com - 2009-02-06

  7. IDRAS - Welcome to the i.DRAS GmbH website

    i.DRAS stands for international, intelligent, individual, innovative and independent solutions for your drug regulatory affairs projects
    products4
    traditional3
    herbal2
    Medical devices2
    medicinal1
    variations1
    CTD1
    DMF1
    drug master file1
    Common Technical document1
    drug regulatory affairs1
    ASMF1
    active substance master file1
    herbal medicinal products1
    human medicinal0
    veterinary medicinal products0

    www.i-dras.com - 2009-02-09

  8. Atlantis BioActives Corporation

    A Canadian-based supplier of biopharmaceutical ingredients extracted from botanical sources and purified within a cGMP compliant manufacturing facility.
    Engineering4
    Cancer3
    Pharmaceutical3
    Breast cancer2
    Pharmaceuticals2
    R&D2
    Cancer treatment2
    Research and development2
    Ovarian cancer1
    Biopharmaceutical1
    Hemlock1
    APIs1
    Cancers1
    Cancer treatments1
    Bioactive1
    paclitaxel1
    Bioactives1
    Drug master file1
    API's1
    taxanes1
    Chemotherapeutics1
    taxane1
    Atlantis bioactives0
    Biopharmaceutical facility0
    cGMP-compliant0
    Cytotoxin paclitaxel0
    Ground hemlock0
    low-cost API0
    Taxane components0
    Taxane extraction0
    Taxus canadensis0

    www.atlantisbioactives.com - 2009-02-07

  9. Drug Master File Management Systems - FDA Pharmaceutical Consulting Firm

    FDA, pharmaceutical, medical device, and biologics regulatory compliance consulting firm.
    Food5
    Administration3
    Drug3
    pharmaceutical3
    compliance3
    medical device2
    regulatory compliance2
    Drug Master File1

    www.dmfmanagementsystems.com - 2009-02-09

  10. Horn Pharmaceutical Consulting - ASMF, Active Substance Master File, US-DMF, Drug Master File, Certificate of suitability, CEP, CTA ,Clinical Trial Applicat ...

    HORN Pharmaceutical Consulting provides regulatory and business advice to companies from the pharmaceutical, biotechnology and medical device industries.
    training5
    pharmaceutical3
    FDA2
    GMP2
    NDA2
    CEP2
    IND1
    CTA1
    GLP1
    QOS1
    GCP1
    Authorities1
    EMEA1
    quality systems1
    CTD1
    BLA1
    SOPs1
    New Drug Application1
    SPCs1
    Drug Master File1
    Common Technical Document1
    Certificate of suitability1
    ASMF1
    regulatory strategies1
    Active Substance Master File1
    Clinical Trial Application1
    US-DMF1
    Biologic License Application0
    CMC-documents0
    European MAA0
    quality overall summaries0

    www.horn-pharma.de - 2009-02-13

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