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  • DrugAge database of compounds that increase lifespan

    DrugAge database of compounds that increase lifespan

    Biomedical Sciences Liverpool August 24, 2015 Check with publisher

    We're starting a new database of drugs and compounds (including natural products) with anti-ageing properties that extend longevity in model organisms. The database will be called DrugAge, and although we have some data already, we are looking for da...

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  • 6-Hour Virtual Seminar on Clinical Data Management - Part II

    6-Hour Virtual Seminar on Clinical Data Management - Part II

    Quality Control, Safety & Security Fremont (California) July 3, 2019 545.00 Dollar US$

    When new drugs or devices are tested in humans, the data generated by, and related to, these trials are known as clinical data. This data represents a huge investment by the biopharmaceutical or device company and is one of its greatest assets. It is...

  • The EU Clinical Trial Regulation - EU Filings & Registrations

    The EU Clinical Trial Regulation - EU Filings & Registrations

    Quality Control, Safety & Security Fremont (California) July 3, 2019 545.00 Dollar US$

    This course covers the requirements for conducting Clinical Studies across the EU via the requirements of the EU Clinical Trial Regulation (for Drugs & Biologics). The course also covers recent updates on EU-GCP associated with the new regulatory...

  • Computational Protein Analysis

    Computational Protein Analysis

    Biology & Physiology Shirley (New York) June 26, 2019 Check with publisher

    Proteins play key roles in almost all biological pathways in a living system, and their functions are determined by the three-dimensional shape of the folded polypeptide chain. Advances in DNA sequencing and structural biology over the years have rev...

  • Biosimilar Testing Services

    Biosimilar Testing Services

    Life Sciences Shirley (New York) June 26, 2019 Check with publisher

    A biosimilar (also known as follow-on biologic or subsequent entry biologic) is a biologic medical product. Biosimilars are officially approved versions of original "innovator" products, and can be manufactured when the original product's patent expi...

  • CYP3A4  peptide

    CYP3A4 peptide

    Immunology Shirley (New York) June 25, 2019 10.00 Dollar US$

    This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases that catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein l...

  • PEGylation Products and Services

    PEGylation Products and Services

    Pharmacology - Drug Development Shirley (New York) May 30, 2019 Check with publisher

    Introducing polyethylene glycol (PEG) to biomolecules and pharmaceuticals is known to enhance stability and pharmacological properties of proteins, peptides, antibody-drug conjugates and small-molecule drugs. As a synthetic polymer with high hydrophi...

  • Generic Drug Services

    Generic Drug Services

    Drug Development Shirley (New York) May 23, 2019 Check with publisher

    The major advantage for generic medicines compared with the innovator counterparts is the cost-benefit, because they do not have to demonstrate the safety and effectiveness through the costly animal and clinical (human) studies that are required for ...

  • Evaluation of Consistency Quality

    Evaluation of Consistency Quality

    Drug Development Shirley (New York) May 23, 2019 Check with publisher

    A generic drug is the formulation that has the same performance as an innovator product, including same dosage, effectiveness, dosage form, strength, quality and other properties. The greatest advantage for a generic drug is far more economical compa...

  • Generics Consistency Evaluation

    Generics Consistency Evaluation

    Drug Development Shirley (New York) May 23, 2019 Check with publisher

    The generic consistency evaluation is composed by quality conformance and efficiency consistency. Evaluation of pharmaceutical quality conformance is defined to determine whether your generic drug preparation and reference formulations are consistent...

  • Registration and Submission

    Registration and Submission

    Drug Development Shirley (New York) May 23, 2019 Check with publisher

    The so-called drug registration and submission represents that the state food and drug administration (FDA), in accordance with the application of the drug registration applicant, makes a systematic evaluation of the safety, effectiveness and quality...

  • CMC Services

    CMC Services

    Drug Development Shirley (New York) May 23, 2019 Check with publisher

    In order to properly manufacture drugs or biologically specific manufacturing processes, product characteristics and product testing must be determined to ensure that products are safe, effective and consistent between batches. These activities are k...

  • Innovative Formulation Technology

    Innovative Formulation Technology

    Drug Development Shirley (New York) May 23, 2019 Check with publisher

    Given the increasingly fierce competition in the pharmaceutical industry, innovative drug delivery systems are now the go-to approach for both new chemical entities development and refinement or repurposing of the approved drug products. Not only for...