We develop solid-state, totally absorbable solid implants TASI, and related technologies for cancers, pain control, etc. 4 key US patents approved in the exciting implantable extended-release technology field. Proof of concept tests is safe and effective with rodent models. Two prototype drug implants are ready for preclinical trial, thanks to a breakthrough technology. Ultimate goal is FDA approval of TASI implants for human prostate cancer, and acute/chronic pain market.

Provider of medical affairs recruiting services for life sciences companies worldwide. TriNet Pharma offers team formation, contract solutions, international solutions, direct-hire solutions, physician recruitment, and concierge staffing services. The company specializes in the pharmaceutical, biotechnology, medical device, and medical diagnostics industries and uses an outcome-based fee structure.

Pharma Advice & Solutions is an independent consulting company which offers, along with its key partners, a fully comprehensive platform to support the medical and pharmaceutical community. The aim of PharmaAS is to provide first class regulatory, medical and clinical services to help clients achieve their goals. Founded in 2017, PharmaAS uses the expertise of consultants who have also been involved in small, medium and large pharmaceutical companies, and the medical sector, at all levels, to ensure all clients’ needs are met. How We Work: PharmaAS and our network of expert partners are fully equipped to be your long-term partner or simply your case-by-case experts. Using our extensive knowledge PharmaAS brings together the brightest teams to ensure your pharmaceutical needs are met. The PharmaAS network offers first class services within the medical and pharmaceutical sector to help small, medium and large companies to advance their plans and realise their regulatory obligations and ambitions. Some of the services offered include: Regulatory Strategy: • Regulatory strategy for all health products and regulatory requirements adapted to each country • Due Diligence of dossiers • Preparation of Scientific Advice meetings Regulatory Registration: • Creation and review of dossiers • Readability User Testing • EU translations Regulatory Maintenance • Marketing Authorisation Applications, registration follow-up, responses to queries • Variations, renewals, transfers • Review of artwork (non) Clinical: • Model Based Drug Development: strategic modeling & simulation based support to the pharmaceutical industry for decision making or regulatory applications • Regulatory support for clinical trials • Creation of expert statements e.g. ERA’s, clinical and non-clinical Overviews • Risk Management Plans • Key Opinion Leader recommendation

Ivory Systems has been a leader in consulting since 1995. Ivory's mission is to deliver results for its Global 1000 clients through the placement of best fit talent for their unique business needs. The Ivory Clinical division has partnered with many pharma and biotech companies in provisioning the brightest talent in the industry. Ivory's relentless focus on delivering results for its clients has made it one of the fastest growing companies in United States.

Engineering & Consulting Services in the domain of Pharma, Biotech & Medical Devices

Expertise in Pharma Research & Development, Manufacturing, Project and Life Cycle Management with specific expertise for Oncology, cardiovascular, CNS, diagnostics, male and female hormonal therapies, dermatology All kinds of small molecules incl. highly potent drugs, radiopharmaceuticals and biologicals (incl. antibodies, proteins, cell and gene therapy) All types of conventional dosage forms, drug delivery and application systems as well as packaging concepts IP generation and defense Preclinical and clinical pharmacokinetics Quality control and bioanalytical concepts Trial medication supply GXP and Quality assurance Change management Training and coaching Services Program and project evaluation for all types of Pharma R&D and Life Cycle Management activities Due diligence for acquisition and in-licensing projects Evaluation and consultancy with special emphasis on biopharmaceutical, pharmacokinetic and CMC (Chemistry, Manufacturing and Control) issues incl. technical transfer assessment IVIVC Project management activities incl. CRO-selection and outsourcing management Independent scientific assessment and expert opinion statements Scientific and technical support at customer site Training, development and educational programs at customer site QP support Organisational development activities efficiency and process analyses design concepts benchmark analyses implementation support Change management projects

Cliniresearchjobs.com is a key job portal specializing in clinical research and healthcare roles, providing global job updates in these sectors. It offers job listings for various positions such as Clinical Research Associate (CRA), Clinical Data Manager, Regulatory Affairs Specialist, Pharmacovigilance, Nursing, and other key roles in clinical trials and healthcare research. The platform is designed to cater to global job seekers interested in the clinical research and healthcare sectors. Regular updates include job opportunities in pharmaceuticals, hospitals, medical device companies, and other healthcare organizations. Free Jobs Posting? Email your requirement details 👉 pharmajobspost@gmail.com Use our whatsApp 👉7978446917

Project Management Consultancy, with an operational focus in Life Sciences, Pharmaceuticals, and Advanced Industries. Our services range from strategic operations consulting through project management, and many aspects in between. Check out our website (www.themoiraeg.com/services) or reach out for more details. We are happy to help find a great solution for your needs.

Welcome to Pharma Udyog - Your Gateway to Pharmaceutical Careers! At Pharma Udyog, we understand the challenges and aspirations of both freshers and experienced professionals in the dynamic pharmaceutical industry. Our mission is to bridge the gap between talent and opportunity by providing comprehensive and up-to-date information about walk-in jobs and vacancies in the pharmaceutical sector. Our Platform: Our user-friendly platform is meticulously designed to cater to the needs of job seekers looking to kickstart or advance their careers in the pharmaceutical field. Whether you're a recent graduate eager to step into the industry or an experienced professional seeking new horizons, PharmaUdyog is your one-stop destination. What We Offer: Tailored Job Listings: Our platform features an extensive range of walk-in job opportunities, specifically curated for the pharmaceutical domain. From research and development to manufacturing and sales, we cover a wide spectrum of roles. Precise Information: We provide detailed information about each job listing, including the location, date, time, and position requirements, ensuring you're well-prepared for your application. Career Insights: Stay informed about industry trends, career growth pathways, and insider tips through our informative articles and resources. Interview Preparation: Our expert guidance on interview preparation and resume-building equips you with the tools needed to excel in the competitive pharmaceutical job market. Why Choose Pharma Udyog? We are not just a job listing platform; we're your career partner. We are committed to helping you find the right opportunities that align with your skills, aspirations, and qualifications. Our dedication to accuracy and reliability ensures that you're always in the know about the latest openings in the pharmaceutical sector. Join Us: Whether you're a fresh graduate excited to embark on your pharmaceutical journey or an industry veteran seeking new challenges, Pharma Udyog welcomes you to explore our platform. Let us be your guiding light as you navigate the vast landscape of pharmaceutical careers. Connect with Pharma Udyog today and take the next step towards a fulfilling and prosperous career in the pharmaceutical industry. 🔆𝗟𝗲𝘁'𝘀 𝗴𝗿𝗼𝘄 𝘁𝗼𝗴𝗲𝘁𝗵𝗲𝗿.

SME App Solution has put together a list of helpful technologies and techniques that may be used in apps to help your business flourish.

P4P Technology is a pharmaceutical company developing a blood plasma substitute based on the plant protein edestin. Our mission is to make advanced treatment and nutrition more accessible by combining natural ingredients with cutting-edge technology to support health, recovery, and longevity. We plan to begin the first human testing by the end of 2025. In parallel, we have launched the dietary supplement Bloody Vital, which uses the same protein and technology as our future IV product — and is already helping hundreds of people improve their health, hormonal balance, and long-term vitality.

Taiho Pharmaceutical, a subsidiary of Otsuka Holdings Co., Ltd., is an R&D-driven specialty pharma focusing on the three fields of oncology, allergy and immunology, and urology. Its corporate philosophy takes the form of a pledge: “We strive to improve human health and contribute to a society enriched by smiles.” In the field of oncology in particular, Taiho Pharmaceutical is known as a leading company in Japan for developing innovative medicines for the treatment of cancer, a reputation that is rapidly expanding through their extensive global R&D efforts. In areas other than oncology, as well, the company creates and markets quality products that effectively treat medical conditions and can help improve people's quality of life. Always putting customers first, Taiho Pharmaceutical also aims to offer consumer healthcare products that support people's efforts to lead fulfilling and rewarding lives.

Provider of clinical pharmacy services intended to assist in clinical documentation services. The company's services provide proclaim billing pathway, claims support, credentialing, contracting, clinical interventions, clinical documentation, pharmacy marketing and also provides a clinical platform, enabling local pharmacies to avail proper tools and methods for empowering them to improve patient outcomes.

With 35 years of experience in the medical device sector, we are passionate about enhancing patient lives through cutting-edge solutions. Our mission is to be your strategic partner in medical device/ SaMD development, guiding you through every phase of your project—from conceptualization and rapid prototyping to successful market launch. Our commitment to excellence is reflected in our deep understanding of regulatory requirements, ensuring that all projects meet the highest quality standards. Together, we can achieve significant progress in healthcare. Certifications: ISO 13485 certified, QMS following FDA 21 CFR Part 820 and MDR ISO/IEC62304, 60601-1, 62366,14971, Services: Product Lifecycle Management Mechanical, Eletrical, and Software Engineering Integration of complexity through Systems Engineering Testing and Quality Engineering Concept Design/Concept Feasibility Design Control, Design Change, Design for Cost, Design for Manufacturing Risk Management Cybersecurity Management Cost/Process Optimization

ClearGuard HD is a device designed to kill infection-causing bacteria inside a hemodialysis catheter hub.

The company primarily operates in the Consulting Services (B2B) industry. Des Pharma Consulting was founded in 2025 and is headquartered in New York, NY.

Regrouper et connecter les diplômés des cycles supérieurs de la Faculté de Pharmacie de l'Université Laval

Provider of healthcare products, services, and technology solutions for improving patient care and operational efficiency. The company distributes pharmaceuticals, medical supplies, and specialty drugs, while offering biopharma services and consulting solutions. Its offerings include automation tools, analytics platforms, and services supporting precision medicine, patient access, and oncology care. Designed to serve pharmacies, health systems, and specialty medical practices.

Janus Data Intelligence develops AI-driven platforms and services for clinical research data processing and analysis. The company focuses on pharmaceutical and clinical trial workflows, helping teams automate data transformation, statistical programming, and reporting. Its offerings include visualization dashboards, Auto SAS programming tools, and AI-equipped biometric services covering coding, writing, and analytics. Solutions integrate with major data capture and storage systems to support regulatory submissions and trial oversight.

Novartis is an innovative medicines company. Every day, working to reimagine medicine to improve and extend people’s lives so that patients, healthcare professionals and societies are empowered in the face of serious disease. Our medicines reach more than 250 million people worldwide. Find out more at https://www.novartis.com See our community guidelines: https://go.novartis.social/3Nboxki

Pharma Focus Europe is a Bi-Annual publication from Ochre Media Pvt. Ltd.

Why Proveris Scientific? Proveris helps pharmaceutical companies developing orally inhaled and nasal drug products (OINDPs) reach the market sooner, saving significant time and money. Proveris believes that developing effective OINDP products requires in-depth knowledge and expertise to understand and control the complex relationships among drug delivery devices, formulations, and human usage that drive product performance. Proveris believes that applying intelligent automation technology, modern data analysis, and proven experimentation techniques leads directly to superior product knowledge and to successful therapies reaching patients far sooner than possible any other way. For more than 20 years, Proveris has worked closely with pharmaceutical companies, device suppliers, contract development, research, and manufacturing organizations, and global regulatory agencies who believe in this focus to elevate the standards in the industry and deliver effective therapies. Proveris does extensive product testing to understand the challenges of developing OINDP products and successfully bringing them to market. By working in its own laboratory and with a broad range of industry influencers, Proveris has unique knowledge and experience in synthesizing the complexities of OINDPs to deliver value-oriented solutions to its customers. Through its patented Proveris by Design™ process, Proveris identifies the human usage performance of an OINDP according to current FDA and ICH guidelines for in vitro testing. Proveris assists with pump, valve, and device selection to optimize effective drug delivery, develops testing strategies, conducts method development studies, and delivers and maintains instruments needed for research and on-going quality assurance testing. Proveris is certified to ISO 9001:2015.