How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval


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How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval uses a practical and hands-on approach to cover the development process of solid oral dosage forms in one single source. How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval uses a practical and hands-on approach to cover the development process of solid oral dosage forms in one single source.

The book details all of the necessary steps from formulation through the post-approval phase and contains industry case studies, real world advice, and troubleshooting tips.


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By merging the latest scientific information with practical instructions, this book provides pharmaceutical scientists in formulation research and development with a concrete look at the key aspects in the development of solid oral dosage forms. Please Note: This is an On Demand product, delivery may take up to 11 working days after payment has been received.

Expertise in Pharmaceutical Process Technology.

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We request your telephone number so we can contact you in the event we have difficulty reaching you via email. We aim to respond to all questions on the same business day. Focuses on important topics, such as robustness, bioavailability, formulation design, continuous processing, stability tests, modified release dosage forms, international guidelines, process scale-up, and much more Part of the Expertise in Pharmaceutical Process Technology series edited by Michael Levin Discusses common, real-world problems and offers both theoretical and practical solutions to these everyday issues Please Note: This is an On Demand product, delivery may take up to 11 working days after payment has been received.

Chapter 1. However, we must ensure that the foundation knowledge that all pharmacists should have is not compromised. The pharmacist, in some instances, is all that stands between the patient and harm from their medicines.

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How to Develop Robust Solid Oral Dosage Forms : Bhavishya Mittal :

This may mean counselling in the correct use of their medicines, but it also means knowing the limitations of types of dosage forms. It is a decade since the National Patient Safety Agency issued guidance on medicines packaging design in a bid to reduce the risk of dispensing errors. But medicines that sound alike or look alike are still responsible for a large proportion of errors. A collaborative approach between manufacturers, regulators and pharmacy organisations is required to tackle the problem.

How to develop robust solid oral dosage forms: from conception to post-approval, by Bhavishya Mittal. Patients who take antihypertensive treatment as separate pills are more likely to continue the therapy than those who take it as a single fixed-dose combination, a study shows.

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    How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval
    How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval
    How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval
    How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval
    How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval

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