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X-ORIGINAL-URL:https://staging.medilinkmidlands.com
X-WR-CALDESC:Events for Medilink Midlands
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DTSTART;TZID=Europe/London:20190902T120000
DTEND;TZID=Europe/London:20190902T160000
DTSTAMP:20260424T003934
CREATED:20190819T121717Z
LAST-MODIFIED:20190819T121717Z
UID:18013-1567425600-1567440000@staging.medilinkmidlands.com
SUMMARY:Clinical Trials Masterclass
DESCRIPTION:CLINICAL TRIALS MASTERCLASS:\nStart with the end in mind \nMonday 2 September\n12 pm – 4 pm\nBoardroom | BioCity\, Nottingham \nPresented by NICE\, Arthur Gallagher and Remap Consulting \nIf you are a biotech company thinking about selling to a larger pharmaceutical company or going to market alone\, it is important that early clinical plans incorporate the needs of the final decision makers\, as well as the regulatory bodies. \nNICE Scientific Advice can help to shape clinical trial protocols and early modelling plans to ensure that evidence generation is targeted at an early to stage to provide the data required at the end of the process\, when a technology is appraised by NICE or other HTA bodies. \nArthur Gallagher will focus on the planning stage of trials and advise when to engage with the Broker and important insurance issues to be aware of. \nRemap Consulting will discuss the importance of obtaining payer scientific advice for achieving pricing and reimbursement success across the EU. \nThis event is free for all based at BioCity and Alderley Park.
URL:https://staging.medilinkmidlands.com/event/clinical-trials-masterclass/
LOCATION:We are Pioneer Group Nottingham\, Innovation Building\, (formerly BioCity)\, Pennyfoot Street\, Nottingham\, NG1 1GF\, United Kingdom
CATEGORIES:Medilink Partner Event
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DTSTART;TZID=Europe/London:20190911T090000
DTEND;TZID=Europe/London:20190911T170000
DTSTAMP:20260424T003934
CREATED:20190722T115331Z
LAST-MODIFIED:20190722T115331Z
UID:17993-1568192400-1568221200@staging.medilinkmidlands.com
SUMMARY:Monitoring and supporting Patients across all healthcare settings
DESCRIPTION:MediWales is collaborating with the West of England Academic Health Science Network (AHSN) to deliver this conference which will focus on monitoring and supporting patients outside the hospital setting (at home\, in nursing and care homes) to specifically enable the measurement of vital signs to calculate a Nation Early Warning Score (NEWS) which is used when delivering care. \nFree delegate places are available to NHS professionals\, research and industry communities\, from both sides of the bridge. We would also like to extend an invitation to companies who have or are developing various approaches to track vital signs. Though this is not about intensive care monitoring – during the event it will be considered how these tools could be used in a community setting. This would include the recording of observations\, dashboards\, wearable devices\, remote monitoring\, devices that aid recording of observation or identifying deterioration with a particular interest in wearable and non-contact tech for those with Learning Disabilities. \nThis event will discuss the challenges and technical issues faced in the community care setting and look at the development of potential clinical / industry collaborations to address the issues in this area. There will also be information on the support and funding available to take projects forward. \nHear from speakers from the AHSN who will present their work on the National Early Warning Score (NEWS) and from Welsh clinical colleagues who will showcase their plan going forward. An insightful look at where automation of technologies and clinical pathways could be accessible to improve an ever evolving process. \nFor further information and to book your place\, please click here.
URL:https://staging.medilinkmidlands.com/event/monitoring-and-supporting-patients-across-all-healthcare-settings/
LOCATION:Coldra Court Hotel\, Chepstow Road\, Langstone\, Newport\, NP18 2LX
CATEGORIES:Medilink Partner Event
ORGANIZER;CN="Medilink Wales":MAILTO:connects-nhs@mediwales.com
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BEGIN:VEVENT
DTSTART;TZID=Europe/London:20190911T160000
DTEND;TZID=Europe/London:20190911T180000
DTSTAMP:20260424T003934
CREATED:20190806T071217Z
LAST-MODIFIED:20190806T071217Z
UID:18004-1568217600-1568224800@staging.medilinkmidlands.com
SUMMARY:Webinar: How do I make the transition from candidate selection through to proof-of-concept?
DESCRIPTION:Join Nikki Whitfield\, VP\, CDMO Services at Quotient Sciences and Claire Thompson\, CEO\, Agility Health Tech and discover how to transition from your candidate selection process and how to utilize a data driven approach to develop the right dosage forms to achieve proof-of-concept. \nThis webinar will explore screening techniques\, integrated approaches and phase-appropriate development strategies. \nLearning Points:\n• What is a suitable screening package for determining the physical properties of an API and what are the red-flags to watch out for?\n• How can the developability classification system (DCS) be used to streamline my formulation development program?\n• How will in-vitro testing and pre-clinical evaluation help me guide the clinical formulation?\n• Will a pre-clinical formulation be suitable for clinical use?\n• Could a simple pharmacy preparation be suitable for my FIH trial or will a manufactured dosage form be required?\n• How can we bridge from pharmacy preparations to GMP solid oral dosage forms that will be robust and scalable?\n• How can you avoid common development pitfalls and ensure future success? \nTo register please click here. \nwww.quotientsciences.com
URL:https://staging.medilinkmidlands.com/event/webinar-how-do-i-make-the-transition-from-candidate-selection-through-to-proof-of-concept/
CATEGORIES:Medilink Partner Event
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DTSTART;TZID=Europe/London:20190917T093000
DTEND;TZID=Europe/London:20190917T163000
DTSTAMP:20260424T003934
CREATED:20190806T073027Z
LAST-MODIFIED:20190806T073027Z
UID:18005-1568712600-1568737800@staging.medilinkmidlands.com
SUMMARY:MPD Training Course: Impact & Assessment of European Medical Device Regulations
DESCRIPTION:Are you ready for the imminent new medical devices regulations applicable from May 2020? Implementation of the new regulations needs to be a priority for industry. In less than 10 months\, medical device regulations are set to change. With such a short timeline\, organisations need to act now to ensure minimal disruption to their organisation and its supply chain. \nMedilink WM\, in conjunction with Acclaim Biomedical Consulting Ltd. is offering a one day workshop to explore the new European regulations for medical devices including; \nThe impact the regulations will have on SMEs\, in regards to costs\nAn overview of the remaining short timeline\nNotified Bodies – impact on SMEs\, and how to overcome potential barriers\nThe changes to CE Marking\nWhy attend? \nBy attending this workshop you will: \nGain a stronger understanding of the new EU regulation structure and its impact to industry\, with a clear practical ‘next steps’ guide.\nFormulate a strategic approach – the immediate actions you need to consider to comply and how to move forward in this new environment\nMeet the expert: \nManaging Director Richard Young has an extensive background in regulatory affairs in addition to GMP (quality assurance)\, GLP (laboratory testing) and GCP (clinical). Spanning over two decades\, these core skill areas have been developed with experience in products ranging from class 3 devices such as Orthopaedic implants (IIb) neurological robots\, through electromedical devices such as infusion systems and cardio vascular products. Richard brings a blend of pragmatism and experience to these disciplines that facilitates insightful problem solving approaches as well as solid solutions. \nRichard’s skills and experience includes such areas as the development and implementation of effective quality management systems\, auditing to ISO and FDA QSIT standards\, and operating at national and international level through industry associations including Eucomed\, ABHI and ABHI Technical Policy Group. \nBooking information: \nDelegate Fee: \nEarly bird fee – Register your place before Friday 23 August and receive a 10% discount \nMember fee: £180+VAT \nNon-Member fee: £215+VAT \nTo secure your place please contact Zoe Heather at zoeh@medilinkwm.co.uk or call 0121 452 5630 \nInvoices will be sent once booking has been confirmed by Medilink WM.
URL:https://staging.medilinkmidlands.com/event/impact-assessment-of-european-medical-device-regulations/
LOCATION:MTIC\, 4 Greenfield Crescent\, Edgbaston\, B15 3BE
CATEGORIES:Medilink Partner Event
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DTSTART;TZID=Europe/London:20190917T100000
DTEND;TZID=Europe/London:20190917T143000
DTSTAMP:20260424T003934
CREATED:20190805T140145Z
LAST-MODIFIED:20190805T140145Z
UID:18003-1568714400-1568730600@staging.medilinkmidlands.com
SUMMARY:WHO Patient Safety Day
DESCRIPTION:WHO Patient Safety Day is an annual event on 17th September. For 2019\, Loughborough University HFE Hub is collaborating with the Healthcare Safety Investigation Branch (HSIB) to offer this free networking event. \nHealthcare staff\, decision-makers\, commissioners\, managers and politicians are all invited. \n10: 00 Tea/Coffee \n10.30 Welcome and Introduction – Sue Hignett & HSIB Director \n11.00 HSIB Presentation – What we have achieved & Going Forward – HSIB Director \n12.  Lunch \n13.00 Panel Discussion \n14.30 Close \nFor further information and to book your place\, please click here.
URL:https://staging.medilinkmidlands.com/event/who-patient-safety-day/
LOCATION:Loughborough University\, Room 101 Schofield Building\, Loughborough\, LE11 3TT
CATEGORIES:Medilink Partner Event
ORGANIZER;CN="Loughborough University":MAILTO:https://billetto.co.uk/e/373129/contact/new
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