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Discover the leading patient adherence pharmaceuticalcompanies. Pharmaceutical Technology has listed the top patient adherence pharmaceuticalcompanies based on our intel, insights and decades-long expertise in the sector. Patient adherence.
Challenge Syner-G was contracted by a US PharmaceuticalCompany to help improve the quality of submission documentation generated during the manufacture of a Drug Substance intended for Phase II trials. Results Syner-G reviewed each documentation and provided suggestions/comments/guidance to the CDMO to bridge the gaps observed.
pharmaceuticalcompany to oversee a 6 month, DS manufacturing as Person-In- Plant (PIP) and assist with preparation of associated submission documents related to Phase III clinical trial batches. Download The Case Study The post Process improvements and in-person monitoring help U.S.
Pharmaceuticalcompanies hold permission to market their products directly to consumers. The direct-to-consumer marketing companies for pharmaceuticals are increasingly moving online as it supports the digitisation of information, enabling patients to take control of their health.
Wholesalers can be either full-line wholesalers, who purchase the complete product line of a company, or specialised companies, which purchase speciality drugs to sell to clinics and hospitals. Selecting the best pharmaceutical wholesalers. Temperature control facilities and supply solutions. Warehousing and logistics services.
The increasing investment in pharmaceutical research and development, and the growing adoption of contract manufacturing and marketing practices are driving the demand for clinical trial contract packaging solutions. Finding the best clinical trial packaging services providers. Clinical trial packaging and labelling solutions.
The surge in diseases is spurring demand for constructive treatment solutions, which is expected to boost the sales of injectable pharmaceuticalcompanies. The document contains detailed information on the suppliers and their product offerings, alongside contact details to aid your purchasing or hiring decision.
The download contains detailed information on the providers and their services and solutions, alongside contact details to aid your purchasing or hiring decision. Prospects of clinical dose companies in contract marketing.
These companies offer services such as formulation development, process optimisation, analytical method development, qualification, validation and testing, regulatory guidance and several other solutions and products. Contract marketing enables pharmaceuticalcompanies to adapt to customer dynamics and value drivers.
Contract marketing companies support pharmaceuticalcompanies in creating, improving, and maintaining their brand, as well as reducing risk, and ensuring better product placement in the market. Identifying the top commercial dose (non-sterile) companies in contract marketing.
The pharmaceutical industry requires specialised and cost-effective commercial packaging solutions to improve efficiency and preserve the integrity of products through the entire supply chain, from primary packaging and labelling to shipping, delivery, storage and distribution to end users.
Find the leading pharmaceutical solid dose manufacturing companies in contract marketing. Pharmaceutical Technology has listed the top solid dose manufacturing companies and solid dose pharmaceuticalcompanies based on our intel, insights and decades-long expertise in the sector.
Pharmaceutical compounding companies are expanding geographically and launching innovative products according to customer requirements to get a better foothold in the market. The document contains detailed information on the suppliers and their product offerings, alongside contact details to aid your purchasing or hiring decision.
Download a PDF of this case study. In 2009, IMPACT (now part of Syner-G BioPharma Group) was contracted by a mid-size global pharmaceuticalcompany to prepare 2 Phase 3 clinical study reports (CSRs) for a biologic agent for the treatment of Crohn’s disease. Establishment of a Long-Term Medical Writing Partnership.
One of the most important components of SRM is the company’s risk appetite statement. This document is approved by the firm’s board of directors and sets the tone for risk-taking at the company by key risks and setting risk tolerances for how much risk the board is willing to take across all business activities. April 2009.
A patient access scheme or commercial arrangement associated with the NICE guidance is a way for pharmaceuticalcompanies to lower the acquisition cost to the NHS to improve its cost-effectiveness, so enabling patients to gain access to high-cost medicine treatments. The NHS price for dupilumab excluding VAT is £1,264.89 Conclusion.
Today, software companies know there is a growing market to meet demand for supply chain visibility platforms. The question for pharmaceuticalcompanies is how they can best deploy their data to make supply chains more efficient. Download the whitepaper on this page to find out more.
Pharmaceuticalcompanies and organisations get access to large amounts of data related to patients, clinical trials, and regulatory affairs. The companies help to design, develop and scale marketing strategies to effectively transition into a digitalised future.
Of the world’s 20 largest pharmaceuticalcompanies, 17 have launched programmes tailored towards increasing medication access in low- and middle-income countries – up from just eight in 2010. Figure 1: Social media posts from pharmaceutical firms mentioning “environment”. A similar theme is evident in company filings.
In addition, several pieces of documentation will be required to support the API qualification, e.g. pharmacopeial compliance. It is also essential to evaluate the reliability of the company supplying the ingredient: do they provide sufficient communication and documentation? Download for a detailed copy of the results.
Consent to begin “Informed consent documents are created to explain to a patient how a trial is going to be run, what they can expect, and the associated risks and potential benefits,” says Jill Balcerzak, Vice President of Global Solutions at content and translations solution provider RWS. The result?
In April, the pilot-level Nordic Pharmaceutical Forum (NPF) initiative, representing Finland, Iceland, Norway, Sweden, and Denmark, released an updated strategy document outlining the region’s plans to establish a joint procurement mechanism for medicines, with a declared focus on advanced therapy medicinal products (ATMPs) such as gene therapies.
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