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The Pharmaceutical Industry is one of the most regulated with specific quality control systems such as Good Laboratory Practice (GLP), Good Clinical Practice (GCP) and Good Manufacture Practice (GMP).
Sound Quality Assurance provides processes and details needed to maintain quality in work throughout the manufacturing process. If the activities are performed in a systematic way and according to the requirements of the QA process the output will be errorless.
While Quality Control helps ensure conformity with third party GMP & GLP compliance auditing and regulatory agency inspections and PAI readiness. All of these processes and procedures support regulatory matters for things like Root Cause Investigations and Corrective & Preventive Actions, and compliance with FDA regulations such as 21CFR Part 11 and Part 820, and FDA Actions such as 483 Observations or Warning Letters.
At Futran Solutions we have developed Standard Operating Procedures (SOP) for our candidate recruitment process which is having end to end process flow of standard recruitment procedures. In this way our team performs all activities in a systematic way and according to the details mentioned in our QA Protocol, so the our output (Solutions and Personnel) also will be staying errorless.
We understand the importance of the client company projects operating under regulatory guidelines and compliance, so does our team. In order to make sure that we can meet our client personnel requirements from QC/QA specialist in this vital sector, as well as to ensure that individuals using our service receive the best solutions and have access to the most relevant employment solutions, we have a team of recruiter dedicated to the Quality Assurance and Quality Control sectors. Our ability to source outstanding talent for QA specialists, QC Scientists and Engineers, and Laboratory Specialists allows us to put together the right team of personnel to support our clients’ Quality and Compliance needs. In order to be as effective as possible for our clients, our QA/QC and Compliance Recruitment Team have developed their knowledge not only in the pharmaceutical manufacturing domain, but also in the employment rules and guidelines at the state and federal level. This keeps current with governmental and industry standards.
Clinical Trials are the validation phases of the Research and Development that were done in the laboratories by the scientific researchers. It is a crucial stage in the overall developmental life cycle of a drug which often takes at least ten years and costs an average of $2.6 billion.
The Clinical Trials process generally runs through 4 Phases with greater numbers of subjects tested during each phase and it may take several years to complete. During these phases, risk management, quality assurance, clinical operations, and regulatory affairs are all monitored and managed by sophisticated clinical trial management systems. Less than 12% of the drugs that make it to Phase 1 trials will ever be approved by the FDA for sale to the consumer.
Only after the Clinical Trials have provided the FDA with their massive amounts of data required to determine the benefits and risks of the potential medicine on the public can a decision be made on whether to grant approval to market the new medicine. Therefore, with the economic impact that is associated with each drug that goes through the process, it is critical to the pharmaceutical firm that these trials prove the efficacy and safety of the medications.
Futran Solutions’ Pharmaceutical and Life Sciences Solutions division, offers firms the specialized skills associated with all phases of the Clinical Trials process.
Being a leading Solutions Provider to the Pharmaceutical sector, our recruitment team has gained advanced knowledge in EMR, Clinical Trials and Clinical Trials Data Management Systems and is capable of understanding your needs in the above functional areas in order to provide our clients the very best resources.
Understanding the functions and interactions of specialized personnel such as Pharmaceutical Clinical Research Officers (CRO), Trial Assistants (CTA), Project Managers (CPM), Data Coordinators (CDC), and Data Managers (CDM) allows us to provide professionals well versed in the team environment they are supporting. Their interactions with Regulatory Affairs specialists assures that the documentation provided meets FDA requirements.Futran Solutions have a proven track record of working across the full clinical research process from drug discovery to launch.
Throughout our time of service in the industry, we have maintained very strong professional affiliations and continued to grow and evolve hand in hand with our clients. It is our clients satisfaction and growth, which drives Futran Solutions’ success as a leading Pharma & Life Science solutions provider globally.Futran Solutions uses its Proprietary method called FARM for effective recruiting process.
Over the past several decades, the pharmaceutical industry has developed and refined its sales and marketing capabilities, marketing major products focused on primary care physicians. While providing a significant revenue source, they are becoming less effective.
The restrictive environment where it is becoming harder to reach those practitioners and the payers are increasing the pressure to lower prices. As a wing of the Pharma Division, our Commercial Operations group touches a very wide area of resourcing needs covering Pharmaceutical Sales, Marketing, & Accounting.
Leaving no stone unturned, Futran specializes in providing perfect Human Capital Solutions for your needs in all of the functional areas of Pharmaceutical Commercial Operations from Sales and Marketing to Medical and Scientific Affairs, E-business to Publication and Planning, Managed Care and Contracting to Procurement, or Competitive Analysis and Strategy to Accounting and Finance. Our team knows how to provide the people and solutions you need.With the experience of successfully sourcing for Commercial Operations positions like Pharmaceutical Production Planner, Director of Commercial Operations, Demand Planning Manager, Content Management Writer, Digital Marketing Manager, Data Analysts, and many more, our capabilities have helped us create a benchmark in quality services rendered to our clients.
Futran Solutions have a proven track record of working across the full life cycle of the pharmaceutical process of drug discovery to launch and commercial operations.
Throughout our time of service in the industry, we have substantially maintained very strong professional affiliations and continued to grow and evolve hand in hand with our clients. It is our clients satisfaction and growth, which drives Futran Solutions’ success as a leading Pharma & Life Science solutions provider globally.Futran Solutions uses its Proprietary method called FARM for effective recruiting process.
While manufacturing automation systems in general have been designed to increase productivity, improve the quality of products, and reduce waste, such systems in the Pharmaceutical environment have even more requirements.
Since the Pharmaceutical industry is highly regulated, the safety of medications and devices sold to the public is of primary importance. Automation Systems for the Pharmaceutical environment require compliance with guidelines such as Good Automated Manufacturing Practice (GAMP) from the International Society of Pharmaceutical Engineering and the FDA’s 21 CFR part 11 regulations. Automated systems may also be designed in compliance with ISA S88 concepts of batch automation and recipe management and be compliant with 21 CFR part 11 features to ensure a structured approach to successful automated manufacturing in a pharmaceutical setting. These systems are tied to Supervisory Control And Data Acquisition (SCADA) devices, Programmable Logic Controllers, Robotic Systems, Distributed Control Systems, Batch Automation Systems, Syncade and DeltaV Systems. Beyond the manufacture of the drugs themselves, automation systems are integral to the process of packaging which includes such steps as weighing, blending, granulating, tableting, capsuling, and filling containers. Systems performing these functions utilize automated inspection machines to ensure the quality of the final product by count, weight, level, vision, etc.
The automated systems doing all of these manufacturing and packing activities integrate with various enterprise systems. The Manufacturing Execution System (MES) which manages the manufacturing resources such as inventory records, product specifications, workflow management and laboratory information is linked to the other systems for Enterprise Resource Planning such as SAP for supply chain management, logistics, finance, and sales. Our years of experience in sourcing the specialized personnel associated with performing in this environment such as Process Automation Engineers, Packaging Engineers, and Pharmaceutical Manufacturing Systems Engineers and Execution Systems Engineers has made Futran Solutions a leader in providing Automation Solutions in the Pharmaceutical sector. Contact us to learn why Futran Solutions is a considered a pioneer of integrated pharmacy solutions offering manufacturing & automation services.
Pharmaceutical Production and Manufacturing have always been a characterized by complex chemical interactions, batch or continuous process manufacturing, automated packaging, and massive amounts of oversight, control, and documentation.
The collection, management, and archiving of the data associated with the materials and processes used and the distribution of the pharmaceuticals as they flow through drug delivery channels to the ultimate consumer requires tremendous planning, extreme care in execution, and detailed documentation. It incorporates numerous functional areas such as Procurement, Production Planning, Packaging, Manufacturing, Supply Chain Management, Batch Automation Systems, and numerous other processes. This complexity is a necessity due to the numerous policies and procedures mandated by regulatory agencies.
This has never been truer than with the advent of Serialization, which mandates tracking and tracing of prescription drugs from the manufacturer to the dispenser. Every step of the Manufacturing Process is recorded, authenticated, archived, and traceable using track and trace technology throughout the manufacture of the drugs and ultimately as they move through the supply chain to the consumer. Skilled personnel such as Raw Material Planners, Production Technicians, Automation Engineers, Process Engineers, Manufacturing Systems Engineers, Packaging Engineers, Procurement, Supply Chain Planners, Materials and Production Planners, Process Engineers, Manufacturing Production Managers, Automation Engineers, and numerous other specialized team members manage every step of the manufacturing and Production process. At Futran Solutions we not only understand the Pharmaceutical Production and Manufacturing, but we excel at working closely with our clients and making sure they have the right people, with the right skills, performing at their highest levels in all of these functions and providing safe and effective prescription drugs to the public.
Futran understands the recent trends in regulatory compliance in the areas of risk, AML and KYC. We have specialized personnel who are trained in the regulatory and risk domain with hands on experience in implementation of regulatory rules such as Basel, CCAR, Dodd Frank and Sarbanes-Oxley.
Tighter credit markets require greater emphasis on IT governance and risk compliance. Leading Financial institutions and banks count on us for effective risk management solutions across their operations in credit risk, operational risk and market risk.
Our extensive experience in the area of credit risk management services and IT governance covers the entire risk management life-cycle including:
● Systematizing and implementing the integrity of rating methodologies
● Netting client and transaction details
● Maintaining and monitoring limits centrally in real-time
● Extraction and Storage of external and internal data
● Messaging and payment (cross-border) solutions
● Enabling Basel-II, III calculations
● Implementation of Dodd Frank and CCAR for larger banks
● Generating pre-defined and adhoc reports
Futran has been an active provider of Wealth Management services by offering a wide variety of skills and experiences. We also provide services to mutual fund companies and private wealth managers. We provide expertise in Multiple Asset Management products and platforms.
Futran Solutions has recognized expertise across multiple asset classes including fixed income, equities, derivatives, currencies, structured products, alternative investments, commodities, precious metals and real state.
Our Wealth Management practices covers functional areas such as:
● Portfolio management
● Asset servicing
● Investment & fund accounting
● Compliance & reporting
Our Retail and Wholesale Banking division adheres to current and innovative solutions in retail banking. We engage in providing technological needs, consultancy and business process sourcing services across various lines of business within the bank. Our team has widespread banking experience with multiple lines of business.
We provide our services in following retail banking areas.
● Cards Technology & Operations
● Loans Origination & Processing
● Mobile & Digital Transformation
● Core Banking Transformation
● Business Analytics
● Risk & Compliance
We provide our service in different verticals of the BFI industries such as Investment Banking.
Providing services and resources in investment banking is the strongest forte of Futran Solutions. Our diverse team includes Business Analysts, Domain Experts and Technical Leads which helps our partners by offering tremendous experience and understanding of investment banking operations.
Futran partners with leading investment banks and financial services firms across the globe, assisting them to take a more tactical approach to their trading processes. With our proven expertise in these areas, we have helped our clients achieve reduced costs of operations with improved service and higher profit margins.
Our proven experience in capital markets & investment banking encompasses all areas including:
● Asset Classes
Futran Solutions Digital Marketing Solutions team is passionate about building effective, strategic digital marketing products that meet your organization’s business goals. Futran Digital Marketing model allow clients to promote their products or brands in more unique way by opening the electronic advertising media via internet, mobile phone, social media and e-billboards. ● Web Design And Development ● Web Design And Development ● Email & Mobile Marketing ● Content Marketing ● Social Media Management
Continuous back-office services, facilities and operational support.Futran Solutions encompasses a set of capabilities for ensuring that enterprise infrastructure and applications are optimized and always available for the business.
● Innovation And Product Development ● Innovation And Product DevelopmenttManaged Support Services ● Infrastructure Services ● Operations And Process Transformation ● Sourcing And Procurement
Coaching by our team of entrepreneurial leaders and over 50 invested mentors. ● TEAM APPROACH ● DIVERSE PERSPECTIVES ● HISTORY OF SUCCESS
Providing customized homegrown Saas solutions or Sourcing solutions using on market-ready technologies. ● Mobile APP Development (IOS/ANDROID/WINDOWS/BLACKBERRY) ● Web APP Design And Development ● DevOps ● Analytics ● UI/UX ● Mean Stack
Recruiting and assembling a team of technologists, executives and business leaders. These team/individual can be onshore or offshore or a combination. Some of the services we offer in :
● IOS ● Android ● Mean Stack ● Full Stack ● DevOps ● UX/UI Experts ● Graphic Designers ● Analytics ● Content Writing
● App Launching ● App Metrics ● Digital Marketing Professionals
Futran Solutions with its rich history and happy clients has been in the forefront of providing best in class pharmaceutical manufacturing and information technology consultants. We have a depth of knowledge in generic IT processes such as data management,software development, project management, operations management, and professional services, that we have developed across multiple industry sectors.
Our managed services provide continuous monitoring of the health of the IT infrastructure and manage its growth while our ability to outsourceIT functionality in a number of essential IT services can reduce costs and provide greater efficiencies. However, when it comes to the pharma sector, we offer much more. Our pharmaceutical industry experience ensures that we can provide you with statistical analysis, reporting services, data analysis and visualization, business analysis, testing and validation specific to your unique needs.
Futran solutions has a great track record in providing resources for cloud transformation, mobile application development, analytics and artificial intelligence. Our people are expert at SAS development, SAP HANA modeling, java development, data warehousing, scientific programming, and data architecture to name just a few of their specialties. To learn more about the innovative array of Information Technology Solutions to your Pharma needs available from futran solutions, please contact us.
● Managed Services – Continuous Monitoring Of The Health Of IT Infrastructure And Managing Growth ● Outsourced IT – An Array Of Essential IT Services And Support ● Professional Services – Implementing IT Systems To Connect And Streamline Business Processes, Systems And Information ● Statistical Analysis ● Reporting Services ● Project Management (Supply Chain Management, IT) ● Data Governance ,Data Analysis, Data Visualization ,Data Sciences ● Programming ,Business Analysis, Testing And Validation
Pharmaceutical Research and Development is extremely complex, time consuming, and expensive. It requires a broad knowledge set that includes not only the issues of the chemical or molecular factors, but their interactions with the body and long term efficacy.
It is not enough just to expand efforts in cell biology, bioinformatics, stem cell research, proteomics / chemoproteomics, synthetic biochemistry, enzymes, receptors, genetics, gel electrophoresis, immunoassays, or numerous other specializations. Rather, it is the ability of research scientists to work with their teams to look at the combination of all of these and many more factors as they develop innovative drugs that their companies can expect to be successful in the marketplace.
When an analytical chemist, biochemist, associate scientist, or senior research scientist is grappling with the many complexities of research and development of a pharmaceutical product, they have not only the science of the matter at hand, but the responsibility of working with their corporate management as well as regulatory organizations in testing, validating, and ultimately distributing an effective and safe drug to the marketplace.
Futran solutions have a proven track record of working across the full spectrum of the clinical research process of drug discovery to launch. Throughout our time of service in the industry, we have substantially maintained very strong professional affiliations and continued to grow and evolve hand in hand with our clients. It is our clients satisfaction and growth, which drives futran solutions’ success as a leading pharma & life science solutions provider globally.
● Bioelectronics ● Cell Biology ● Stem Cells ● BioTechnology ● Phenotypic Screening ● Structural Biology ● Cancer Immunotherapy ● Bioinformatics ● Proteomics/ Chemoproteomics ● Biomarkers ● Synthetic Biochemistry ● Enzymes, Receptors, & Genetics ● Safety, Quality And Efficacy Tests ● Analytical Method Development ● GPC/SEC – HPLC, RP – HPLC, Gel Electrophoresis, Immunoassays, IEF, MS, CD, CE,ELISA
It was not until 1961 that the disaster caused by a medicine promoted for use by pregnant mothers known as thalidomide, prompted the first systematic international efforts to address drug safety. Since then, numerous local, national, and international agencies have been established to monitor the efficacy and safety of medications on the worldwide population.
In response to this the pharmaceutical industry has made great efforts in the advancement of pharmacoepidemiology which combines pharmacology as the study of the effect of drugs and epidemiology as the study of the distribution and determinants of diseases in populations. This effort to study the effects of drugs on large numbers of people also includes the unique area pharmacovigilance, which provides for continuous monitoring for unwanted effects and other safety related aspects of drugs that are already on the market.
These issues require medical information systems that are designed to provide the greatest degree of thoroughness in the detail required to support the global medical information. Specialized medical writing, regulatory reporting, drug safety compliance, medical inquiry support, risk management, safety database administration, and individual case study report capture are essential functions in this endeavor.
In order to support such highly specialized monitoring and reporting matters uniquely skilled professionals such as drug safety specialists, medical advisors of product safety, medical writers, safety risk leads, and drug safety associates are deployed. As for pharmacovigilance, which has its own unique requirements, specialized pharmacovigilance operations managers, safety managers, principal scientists, systems managers, and administrators are needed to provide the oversight and reporting that is essential to the monitoring agencies. Futran solutions’ has the depth of experience in these functional and operational areas to ensure that your organization can meet its monitoring and reporting requirements.
● Global Medical Information ● Pharmacovigilance ● Medical Writing ● Product Complaints ● Drug Safety ● Pharmacoepidemiology ● Medical (Healthcare Professional) Inquiries ● Individual Case Study Report Capture And Processing ● Literature Screening ● Signal Detection And Assessment ● Risk Management ● Periodic Safety Writing ● Regulatory Expedited Reporting ● Safety Database
Process validation is the establishment of documented evidence, which provides a high degree of assurance that a specific process (Computer System / Pharmaceutical Manufacturing Process) will consistently produce a product meeting its predetermined specifications.
As Futran Solutions our Specific Process is known as Rare and Unique Skills Hunting (RUSH) and our Validation Protocol helps us to produce outcomes which meet predetermined client requirements specifications. We understand the importance of Process Validation and utilize it to ensure the highest quality of service in our solutions to our clients which result in:
● Quality assurance cost reduction ● Customer satisfaction ● Fewer product recalls ● Fewer batch failures ● Decreases risk of regulatory noncompliance ● Smooth running of process ● Less in process control and end product testing
We also understand the prerequisites for successful validation. Our recruitment team is specialized in domain and fully experienced to hire resources such as Pharma Validation Engineers, Pharma Computer Systems validation specialists, Pharma Validation Auditors, Pharma Validation – Project Managers, Pharma Validation Specialists, Pharma Validation – Inventory Optimization Analysts, Pharma Technical Writers, Pharma LIMS Developers, Pharma Equipment Validation specialists, Pharma QA Validation Engineers etc. and we make sure that the resources we provide are experts with experience in planning, understanding & communication, training SOP’s instrument & methodologies, validation master plan, data analysis and validation reports.
FUNCTIONAL AREAS WE SUPPORT:
● Computer System Validation ,Process Validation ● Equipment Qualification ,Cleaning Validation ● Analytical And Microbiological Methods Validation, Validation Program Development ● Validation Planning ,Vendor Auditing ● Risk Assessment And Mitigation ,User Requirements Gathering And Documentation ● System Design Documentation (FRS, DS) ,Qualification Protocol (IQ, OQ, PQ) Development. ● LIMS, ERP/MRP, CRM, CMMS, SAS,And ORACLE Clinical.