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.

Functional Areas We Support:

• Quality Assurance
• Quality Control
• GMP & GLP Compliance Auditing
• FDA Action (483 Observations, Warning Letters, Consent Decrees) Remediation
• FDA Compliance With 21CFR Part 11 And Part 820
• Policy, SOP, & Batch Record Review, Creation & Optimization
• Quality System (QS) Development, Assessment & Optimization
• Raw Materials ,API And Spectroscopy
• HPLC ,Assay
• IPQC (In Process Quality Control)
• Root Cause Investigations & Corrective & Preventive Action (CAPA)
• Planning & Execution

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. 

Functional Areas We Support:

• Risk Management
• Medical Writing
• Quality Assurance
• Clinical Operations
• Biometrics/Clinical IT
• Regulatory Affairs
• Clinical Trial Management Systems

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. 

Functional Areas We Support:

• Market And Competitive Analysis And Strategies
• Publication Plans
• Promotional Tactics And Brand Marketing
• Medical And Scientific Affairs
• Sales And Marketing
• Managed Care And Contracting
• E-Business
• Procurement And Purchase
• Accounting And Finance
• Production Planning/Buyer

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.  

Functional Areas We Support:

• SAP-Supply Chain Management
• Supervisory Control And Data Acquisition (SCADA)
• Programmable Logic Controllers (PLC)
• Distributed Control Systems (DCS)
• Batch Automation Systems
• Syncade And DeltaV Systems

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.   

Functional Areas We Support:

• Packaging
• CIP/SIP/COP
• Production Planning
• GMP,CGMP
• Drug Manufacturing
• Manufacturing
• Protein Drug Products
• Radiopharmaceutical Manufacturing
• Drug Delivery

Risk

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.

Compliance

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.

● Payments

● 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:

● Pre–Trade

● Trade

● Post-Trade

● Asset Classes