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Service Level Agreements Home / Stability Storage Solutions / Storage / Photostability Photostability Testing as per the ICH Q1B guidelines should play a vital part of new pharmaceutical substance and drug products. In line with the ICH Q1B guidelines our photostability testing will perform to specification in normal ambient temperatures of up to 21ºC and…
Read MoreService Level Agreements Home / Stability Storage Solutions / Storage / Disaster Recovery Do you have a disaster recovery plan? Source Stability Storage Solutions are your perfect partner to support you with your disaster recovery planning. We can help protect your samples when facing internal threats such as power outages or equipment failure as well as external threats…
Read MoreService Level Agreements Home / Stability Storage Solutions / Validation Services Source Stability Storage Solutions offers validation services including an online secure portal which gives full access to accurate remote monitoring and mapping with a full audit trail and automatic report generation directly from our environmental cabinets, reach-in rooms, walk in rooms, and cold rooms.…
Read MoreService Level Agreements Home / Stability Storage Solutions / Service Level Agreements Source BioScience is a Market-leader in Service and Validation Service and maintenance from Source Stability Storage Solutions is tailored to individual customer’s requirements and designed to suit a full range of equipment. With over 30 years experience our engineers have an extensive knowledge…
Read MoreSanger Sequencing Home / Genomics / Sanger Sequencing Delivering unrivalled turnaround times for Sequencing using our streamlined SpeedREAD™ data delivery system. Providing high-quality data retrieval within 12 hours from sample receipt. Sanger Sequencing With over 20 years experience providing market-leading Sanger Sequencing services to the Life Science space, Source Genomics are fully-equipped to guide and…
Read MoreSource BioScience completes £18.5m strategic acquisition of LDPath Ltd
Read MoreIntroduction Stability storage is undertaken on a variety of pharmaceutical products including tablets, capsules, liquids, creams, gels and a variety of medical devices. As part of the stability storage trial, products are stored in equipment to replicate various environmental conditions, and at various time points, those products are subject to a variety of analytical tests…
Read MoreHelping you differentiate between IQ, OQ and PQ and decide what is right for you. Regulations require that quality is ensured throughout the life cycle of a product. This means that manufacturers are responsible for product quality from manufacture to until it is used by the patient. This requirement is standardised under EU regulations as…
Read MoreIntroduction Stability storage is a key process in bringing a pharmaceutical product to market. Fundamentally, the objective of stability storage trials is to determine and substantiate the shelf life of the product and packaging, and to verify that the API’S (active pharmaceutical ingredients) do not deteriorate over time, given those environmental conditions. Why outsource? A…
Read MoreA large number of drug products are light sensitive and therefore their formulated products may degrade during manufacturing, storage, and administration. This could result in potency loss, altered efficacy, and adverse biological effects. Testing guidelines for potential photolabile substances are described in ICH Q1B and aim to standardise the procedure used to establish and demonstrate that, as…
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