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  1. 1
    General introduction to non-clinical toxicity testing of pharmaceuticals

    General introduction to non-clinical toxicity testing of pharmaceuticals

    Published 2016
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  2. 2
    SOPs and improving business performance to meet GXP

    SOPs and improving business performance to meet GXP

    Published 2013
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  3. 3
    Procedural assessments of SOPs to ensure SOPs are logical and meet GXP requirements

    Procedural assessments of SOPs to ensure SOPs are logical and meet GXP requirements

    Published 2013
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  4. 4
    Principles of SOPs and hierarchy of documents

    Principles of SOPs and hierarchy of documents

    Published 2013
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  5. 5
    Effective SOP writing

    Effective SOP writing

    Published 2013
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  6. 6
    Use of technology and document management systems for SOPs

    Use of technology and document management systems for SOPs

    Published 2013
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  7. 7
    Electronic SOPs vs. paper compliance with FDA CFR 21 part 11 /

    Electronic SOPs vs. paper compliance with FDA CFR 21 part 11 /

    Published 2013
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  8. 8
    SOPs as part of the quality system

    SOPs as part of the quality system

    Published 2013
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  9. 9
    Vaccine preclinical studies part 1 of 2 /

    Vaccine preclinical studies part 1 of 2 /

    Published 2015
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  10. 10
    Vaccine manufacturing part 2 of 2 /

    Vaccine manufacturing part 2 of 2 /

    Published 2015
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  11. 11
    Regulatory considerations for vaccine development, talk 2 clinical regulatory considerations (part 1 of 2) /

    Regulatory considerations for vaccine development, talk 2 clinical regulatory considerations (part 1 of 2) /

    Published 2015
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  12. 12
    Regulatory considerations for vaccine development, talk 1 chemistry, manufacturing and control /

    Regulatory considerations for vaccine development, talk 1 chemistry, manufacturing and control /

    Published 2015
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  13. 13
    Regulatory considerations for vaccine development, talk 2 clinical regulatory considerations (part 2 of 2) /

    Regulatory considerations for vaccine development, talk 2 clinical regulatory considerations (part 2 of 2) /

    Published 2015
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  14. 14
    Vaccine preclinical studies part 2 of 2 /

    Vaccine preclinical studies part 2 of 2 /

    Published 2015
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  15. 15
    Nursing support of families and carers of people with dementia

    Nursing support of families and carers of people with dementia

    Published 2017
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  16. 16
    Complement diagnostics

    Complement diagnostics

    Published 2017
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  17. 17
    Treatment effect estimates in multi-arm multi-stage (MAMS) clinical trials

    Treatment effect estimates in multi-arm multi-stage (MAMS) clinical trials

    Published 2020
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  18. 18
    Ultrafiltration a practical overview /

    Ultrafiltration a practical overview /

    Published 2020
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  19. 19
    Overview of nonclinical safety assessment

    Overview of nonclinical safety assessment

    Published 2020
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  20. 20
    Approaches to nonclinical vaccine development

    Approaches to nonclinical vaccine development

    Published 2021
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