56223 Courses delivered Online

Good Manufacturing Practice (GMP) is a set of rules for medicines manufacturers to follow so that their products are safe, effective, and of good quality. Everyone who works in a processing, quality control, packaging, or warehouse environment for a pharmaceutical or biotechnology company, or one of their contractors, must understand why GMP is important, how it applies to them, and how to comply with it. This short course explains what GMP is and why it is important, and it gives some lessons from history. It introduces the regulations and guidance documents that are the source of GMP rules. Finally, it touches on regulatory inspections and the consequences that can arise from failure to comply with GMP requirements.

Unschooling 101 is a webinar that sets out the nuts and bolts of unschooling and how you can actively prepare yourself and your child for the journey ahead.

Reporting to the LA when your child is in burnout

Unschooling PDA children

It is common for unschooled, or Self Directed Learners, to learn to read anywhere between the age of 3 - 16 years old. How can you be sure that your child will learn to read and that unschooling reading works? This webinar will draw attention to the things that children do that are developing the skills and building the foundations that they need for them to learn to read.  This will be done through using real life examples and stories from the unschooling community of real children who have learnt to read in their own time and in their own way.  This webinar is FREE for LPL Monthly Members along with a back catalogue of Unschooling Webinars, 2 live webinars a month, and discounts on coaching and mentoring services. Sign up for just £20 per month. Yes! I want to join the LPL Monthly Membership

Clinical trial protocols are an essential part of clinical trial design. Protocol documents are critical to conducting safe and cost-effective investigations. Protocol documents are large and complex, containing comprehensive information relating to purpose, design and conduct of a clinical trial. Aspects of a protocol include patient eligibility criteria, and treatment specifications. This short course provides an overview of clinical trial protocols. Opportunities to improve a clinical trial protocol for regulatory approval are also discussed.

New drug development requires major investment in capital, human resources and technical expertise. Strict adherence to regulations on testing and manufacturing standards is also required before a new drug can be marketed. One of the greatest challenges in conducting clinical trials is that of efficiency. As trials become more comprehensive, involving large numbers of participants globally, their duration is prolonged and costs increase. The longer trials last, the shorter is the patent life remaining after market approval and the longer patients must wait for the new product. This short course covers the key components of clinical trials and how these requirements interact with the drug development cycle.

For individuals who are not accounting specialists, the budgeting process can be a mysterious and frightening experience. This course seeks to dispel the myths and misunderstandings around budgeting by describing the process and its significance in simple terms.

What is this webinar about? This webinar will provide an introduction to treatments for the collection of psychological challenges known as Post Traumatic Stress Disorder (PTSD) from a CBT / psychotherapeutic perspective. This will include looking at the goals of treatment and the techniques used to achieve them by working collaboratively and compassionately with clients. Key Topics Understanding Trauma and Trauma Informed Symptoms of PTSD and Complex PTSD Measuring PTSD severity and impact Goals in treating PTSD EMDR Key Therapeutic Techniques Latest research on PTSD What have previous attendees at 'Treating PTSD' said about the workshop? Lots of useful insight into subject matter. Really helpful course As someone who has just qualified in CBT, I have found this to be a brilliant course supplementing my knowledge and providing creative treatment options. I particularly like the detailed tips provided throughout the course about how best to practice. I have learned so much today and found it very insightful, educational and in particular the research stats too. I felt engaged throughout and greatly appreciate this opportunity and look forward to many more to come. Very insightful learning, it has increased my understanding of how to facilitate therapeutic process to address symptoms of PTSD. Much appreciated. I’m new to this as I’m a Counselling Student and found it extremely interesting and useful.

Informed consent in clinical research is an ethical and regulatory requirement. A research subject must enter a study voluntarily, be informed about risks and benefits, and understand the difference between investigation and treatment. Subjects must not be coerced into enrolment, nor must they be enticed by exaggerated claims of benefit. Before they can enrol, all potential subjects must agree, in writing, to participate. In addition to ethical and regulatory imperatives, the potential for litigation by subjects further highlights the importance of rigorous adherence to informed consent principles. In this short course we set out the principles and requirements and provide examples of practical issues confronting healthcare professionals and subjects.