Skip to main content

Shopping Cart

You're getting the VIP treatment!

Item(s) unavailable for purchase
Please review your cart. You can remove the unavailable item(s) now or we'll automatically remove it at Checkout.
itemsitem
itemsitem

Recommended For You

Loading...


“helena mayer”

Showing 1 - 12 of 12 results for “helena mayer”
Skip side bar filters
  • How to Start a Blood-grouping Reagents Business (Beginners Guide)

    by Mayer Helena ...
    This publication, published by SamEnrico, covers How to Start a Blood-grouping Reagents Business (Beginners Guide) ... Read more

    $19.79 CAD

  • How to Start a Blood-grouping Reagents Business (Beginners Guide)

    by Mayer Helena ...
    This publication, published by SamEnrico, covers an overview of How to Start a Blood-grouping Reagents Business (Beginners Guide) . The text has been edited and prepared for general readership. All content within is protected by copyright and may not be reproduced, distributed, or transmitted in any form without the prior written permission of the copyright holder. ... Read more

    $28.79 CAD

  • Audiobook

    Phineas and Ferb Chapter Book Set (Books 1-3)

    Speed Demons, Runaway Hit, and Wild Surprise

    Unabridged

    3 hours 25 min

    School’s out for the summer, and stepbrothers Phineas and Ferb decide to make each day an adventure! This audiobook collection contains the first three books in the bestselling Phineas and Ferb chapter book series: Speed Demons, Runaway Hit, and Wild Surprise. Perfect for fans of the hilarious hit show!Phineas and Ferb #1: Speed DemonsIt’s summer vacation for Phineas and Ferb, and they have a lot ... Read more

    $19.00 CAD

People who read these also enjoyed

  • Clinical Research Coordinator Handbook, Fourth Edition

    In this fully revised and expanded fourth edition of the essential reference for clinical research coordinators, Deborrah Norris provides expanded coverage of CRC duties and regulatory requirements, including new sections on investigator responsibilities, data clarification, and adverse event reporting. The books five appendices include a directory of CRC resources, updated forms and checklists, ... Read more

    $9.61 CAD or Free with Kobo Plus

  • Clinical Research Coordinator Handbook, 5th edition

    “This extremely useful title is written for anyone planning to implement clinical trials at an institution. … the author has carefully detailed the types of forms, study records, and case report forms. … A powerful appendix and glossary of relevant terms help make this a needed book for any clinical trials office.”— Journal of Hospital LibrarianshipIn this fully revised and expanded fifth edition ... Read more

    $13.73 CAD or Free with Kobo Plus

  • Cobert's Manual Of Drug Safety And Pharmacovigilance (Third Edition)

    Completely revised and updated, Cobert's Manual of Drug Safety and Pharmacovigilance, Third Edition, is a how-to manual for those working in the fields of drug safety, clinical research, pharmacology, regulatory affairs, risk management, quality/compliance, and in government and legal professions.This comprehensive and practical guide discusses the theory and the practicalities of drug safety ... Read more

    $50.59 CAD

  • The Combination Products Handbook

    A Practical Guide for Combination Products and Other Combined Use Systems

    Edited by Susan Neadle ...
    Combination products are therapeutic and diagnostic products that combine drugs, devices, and/or biological products. According to the US Food and Drug Administration (FDA), “a combination product is one composed of any combination of a drug and a device; a biological product and a device; a drug and a biological product; or a drug, device and a biological product.” Examples include prefilled ... Read more

    $114.04 CAD

  • Process Architecture in Biomanufacturing Facility Design

    Essential information for architects, designers, engineers, equipment suppliers, and other professionals who are working in or entering the biopharmaceutical manufacturing fieldBiomanufacturing facilities that are designed and built today are radically different than in the past. The vital information and knowledge needed to design and construct these increasingly sophisticated biopharmaceutical ... Read more

    $213.99 CAD

  • Good Design Practices for GMP Pharmaceutical Facilities

    Edited by Terry Jacobs ...
    Series series Drugs and the Pharmaceutical Sciences
    This revised publication serves as a handy and current reference for professionals engaged in planning, designing, building, validating and maintaining modern cGMP pharmaceutical manufacturing facilities in the U.S. and internationally. The new edition expands on facility planning, with a focus on the ever-growing need to modify existing legacy facilities, and on current trends in pharmaceutical ... Read more

    $97.55 CAD

  • How to Validate a Pharmaceutical Process

    Series series Expertise in Pharmaceutical Process Technology
    How to Validate a Pharmaceutical Process provides a "how to approach to developing and implementing a sustainable pharmaceutical process validation program. The latest volume in the Expertise in Pharmaceutical Process Technology Series, this book illustrates the methods and reasoning behind processes and protocols. It also addresses practical problems and offers solutions to qualify and validate a ... Read more

    $44.79 CAD

  • Current Good Manufacturing Practices (cGMP) for Pharmaceutical Products

    This Book contains 11 Modules of Current Good Manufacturing Practices (cGMP) requirements for pharmaceutical industry which will be very useful for job seekers in Pharma sector, Beginners and Learners of a Pharmaceutical industry and Pharmacy Students. It is a must-read book for every students aspiring for Placement in any pharmaceutical industry ... Read more

    $9.99 CAD or Free with Kobo Plus

  • Design Controls for the Medical Device Industry, Third Edition

    This third edition provides a substantial comprehensive review of the latest design control requirements, as well as proven tools and techniques to ensure a company's design control program evolves in accordance with current industry practice. It assists in the development of an effective design control program that not only satisfies the US FDA Quality Systems Regulation (QSR) and 13485:2016 ... Read more

    $336.66 CAD