Food Safety Measures – Are they Enough?

As per Food Safety and Standards Authority of India( FSSAI ) promotion of general awareness about food safety and food standards is very important in India to improve the food quality. FSSAI lays down mechanisms and guidelines for accreditation of certification bodies engaged in certification of food safety management system for food businesses. It also provides training programs for people who intend to get into food business.

It has not become mandatory to get a license and certificate from FSSAI before getting into food industry. This step has been initiated for the safety of consumers who are still not well aware of the safety measures. Due to the strict licensing rules, there is a rise in the need for FSSAI Consultant in India. These consultants help with Food Licensing & Registration in India. They review all the paperwork, form and apply on the client’s behalf.

Getting a Food License from FSSAI is not an easy task. It involves lot of paper work and food quality check. Despite of all these measures by the Indian government there is still a question mark on the consumers’ safety. Are they actually well aware of the measures to be taken before consuming a product? Are they aware of interpreting the information on food labels? These questions give rise to need of making consumers aware of the measures to be taken at their end.

Food Security Consultant

In the new age of entrepreneurship we are more or less aligned to opportunities that are rare and fruitful. The ideology of young entrepreneurs are to deliver perfect operations with minimal wastage of resources. The optimization of resources to provide food related operations is a major challenge faced by industries. To overcome such difficulties and inculcate refined operations FSSAI has taken the lead and developed food security consultants across India.

The FSSAI jointly with various organizations is working to provide industry standard consultants. Those consultants would be highly functional in food security and licensing. And even certified as FSSAI Consultant in India. The outlook of food industry could majorly be dependent on FSSAI consultants. Nurturing talented people and delivering the best in industry talent is the major challenge to overcome by FSSAI.

The food processing and food licensing industry of India is surrounded by a lot of sectors interconnected and dependent upon it. In order to handle the challenges a lot of major authorities are operating. The Food Licensing & Registration in India is monitored and controlled by FCI. FCI and FSSAI both take the responsibility of standardising and regularising the food industry

International Business in Pharmaceutical Sector

Businesses worldwide aim to extend their client base globally. On the same platform Pharmaceutical Companies are aiming high to outreach International markets in ES,UK and other south Asian markets. Expanding business invites a lot of hurdles and difficulties to achieve the stipulated targets.  Industries catering Pharmaceutical companies are running on point base outsourcing schemes. They tend to enter markets with a single Sourcing Partner Of Injectableplants For EU & UK.

Achieving those stipulated targets Pharmaceutical companies are considering to take in Sourcing Partner Of Contract Manufacturing For UK. So whenever a certain demand arises in UK markets, the burden on the parent company diminishes resource wise and monetary wise. Therefore, making a substantial part of efforts resourceful and efficient.  The demand for pharmaceutical sector is on an up rise as people are more inclined to them intended to their research.

In India the markets are never saturated, so we can outlay our industry. The government on the other hand is traditionalising a new concept of Make In India to promote our Industrial growth. Rendering to this advancement there is a need to develop Sourcing Partner Of MHRA Approval Plants in India. Collectively these efforts would lead to advancement in Indian industries operating worldwide. We being the sourcing partner of contract manufacturing for UK pharmaceutical sector, is encouraging more research related work.

Pharma consultants – The right solution

India, out of all the developing countries, is the one with the strongest and most developed pharmaceutical industry. This industry has been an aid to the country’s economy.  There are many reasons behind this attraction towards Indian pharmaceutical industry. Few of the reasons are highly – skilled doctors, trained professional staff and strong research & development infrastructure.

This growth of Indian pharmaceutical industry is due to the changes in import regulations.  Though the import rules are quite stringent, there are many companies, which help in getting the NOC for Import in the industry.  This has let to an inflow of advanced technology in the country.

These pharma consultants help with Embassy Attestation and to meet the government requirement related to the rules and regulations for the same. Rihim Pharma Consultants and Pvt. Ltd. help with Embassy Attestation For Pharma Industry in Delhi.  This company is the solutions to all the problems related to Regulatory Affairs at the office of the Drug Controller General (India), New Delhi.

In a country like India, where pharmaceutical business is on boom, such consultants have come up as a blessing in disguise. With various astounding activities of the Indian government, the Indian prospective pharmaceutical industry seems to have a great scope for drawing in more outside ventures.

NEED FOR EMBASSY ATTESTION FOR IMPORT PURPOSES

Indian Medicine Industry is a high yielding market producing a superior quality of drugs for a global usage. Indian Pharma market is also known as one of the fastest growing market all over the world. In the past decade there has been a massive development which  seen in the globalization of the pharma industry. Indian pharma industry is facing a huge challenge for penetration due to this globalization. There are a number of reasons which makes it comparatively difficult for the new pharma company’s to establish their presence in the market. Challenges like Competition from Generics, High Health care cost, increasing cost of Research and development, stringent price control etc. which is why more and more international companies are stepping into the Indian market. For establishment of a foreign company for introducing any new drug or test a NOC for Import is required.

There is a list of separate provisions involved in licensing for drug importation. This is because a particular drug  is used in varied quantity by various establishments like Testing & research institutes, Govt Hospitals, clinical researches etc . The Pharma Act of 1948 governs the pharma profession in India for domestic consumption.

For authenticating a drug in the market it becomes very important for any pharma company to get Embassy Attestation for the consumption of any drug. In the absence of this attestation it becomes extremely difficult for the company to penetrate as they don’t have any legitimacy or proof of authenticity attached with that new or improved drug.

In order to complete the vivid process of pharma regulation there are an array of Govermental organizations involved while getting an Embassy Attestation for Pharma Industry in Delhi. The various embassies have various rules and regulations which are to be followed for importing any pharma product. It involves a long and tiresome job of filling various documents and following a lengthy process. In order to ease this process RIHIM pharma has a team of trained professionals who are always on their toes to assist their client with each and every aspect of licensing processing involved.

GENERIC DRUGS IN INDIA: Laws for Registration and Certification.

The gubernatorial situation associated with pharma and drug Industry of India has seen a rapid change in a small period of time wherein DCGI is arriving up with particular directives related to the narcotic policies every now and then. The certification related to pharma signing up is at par with that off US FDA and DCGI is targeted at generating the kind of data which is appropriate on global level. The constant change of rules and Pharma Regulatory Affairs requires professional to provide the current needs of both the current and new drug organizations to effectively release their therapeutic products in the Native Indian industry.

In purchase to gain achievements by presenting a new medication it becomes crucial for the organizations to reduce time taken while releasing the item in the marketplace, as for every medication released there are many opponents but achievements comes to only those organizations who start the utilization in regular basis. Keeping this vital problem in mind RIHIM pharma has appeared as well known Drug Regulatory Consultant in India. They support their client in each and every procedure engaged at various stages of item signing up and acceptance. RIHIM has helped several pharma manufacturers/ importers, authorities, preclinical Equipment users and Medical trial organizations in the procedure of signing up with DCGI.

There are various steps for seeking authorization to transfer or produce a new medication in the Native indian industry. Many a times the regulating mortgage approvals often appear as a barrier for the firms in the release of a new medication in the marketplace. To ease the reasons engaged in this procedure there are many Drug signing up professionals available in the Native indian industry that support the organizations starting from the signing up to the release of the medications, medical studies, therapeutic accessories etc. There isn’t any specified period of your energy and effort mentioned in this procedure which is another big problem in getting the acceptance on your own, therefore in-order to make the procedure of signing up quick and straight forward RIHIM has their specific team of individuals who act as per the recommendations of DCGI and get the acceptance faster and easier for their clients. 

Food Safety: Not in risky hands

Who doesn’t crave the mouth-watering roadside street food like golgappas, alootikkis, momos, etc., but with a doubt that if it is hygienic enough or not, yet we can’t stop ourselves. Though Food Safety and Standards Authority of India has formulated guidelines to regulate this unorganized sector, Delhi government has failed to effectively implement them. Now, the street vendors, themselves, are coming together to ensure acceptable standards of food quality and hygiene.

Food Licensing & Registration in India has been created for laying down science based standards for articles of food and to regulate their manufacture, storage, distribution, sale and import to ensure availability of safe and wholesome food for human consumption.

FSSAI certificate has now become mandatory for all manufactures, traders, restaurants and those who are involved in food business, commonly termed as Food Business Operators.

Delhi was one of the first states to implement the Food Safety and Standards Act 2006. But sources in FSSAI claim it has failed to deliver the goods.There is a need to create awareness about food safety among public and street vendors. If customers demand it, they will be forced to maintain hygiene. This will result in increase in their monthly income as they can charge more for providing good quality food. FSSAI Consultant in India has been working to ensure the food safety in India and have done a lot of work to streamline food standards, hygiene and quality, all across India.

India - Strong Pharma Destination

India is pronto becoming one of the best-considered settings for global pharma's drug research and development (R&D). Many factors have contributed to this deploy attraction, namely: highly-skilled doctors, trained paramedical staff, and a strong research infrastructure.

Pharma Licensing Consultant firms attribute the growth in pharma sales to transitional disease profiles, bigger access to medicines, and growing public health programs, and if the Indian economy keeps on growing, the local pharmaceutical market will experience a huge transformation in the years to come, reaching the top 10 around the year 2015. This will definitely have an impact on the global pharma industry in regards to R&D.

There are various reasons as to why India is such a desired location for research and development:

India is expected to be the most populated country by 2035, turning it into the youngest one. It holds 20% of the world's population under 24.

This country has a varied patient population in regards to race, culture, and economic level; and many are inexperienced about treatment. They are less prepared to deal with pneumonia, Hepatitis B, diabetes, or cancer, thus, the more patients, the higher recruitment quota. Shorter recruitment timelines prevail in India and patients' compliance is higher, that’s where firms like Drug Regulatory Consultant in India comes to light.

Many of the issues regarding patent protection and intellectual property rights are settled. India is compliant with the Trade Related Intellectual Property Rights Act (TRIPS). It holds a first-class data-processing infrastructure for biostatistics and bioinformatics, and huge generic drug-manufacturing facilities.

All of these are critical aspects for R&D costs, which have dramatically been increasing for the past few years. It is vital to streamline the development process as much as possible.DCGI Consultant in Delhi/India provides a great base for Pharmaceutical consulting firms.

Outsourcing Regulatory Affairs Services

For companies exploring the prospects of the global marketplace, understanding each country's regulatory requirements can be a difficult and time consuming task. With the changing regulatory scenarios of many developed and less developed nations, companies are finding it difficult to maintain the required in-house regulatory staff to ensure compliance across borders.

These significant changes in government regulations, market conditions and technology is forcing pharmaceutical and biotechnology companies of all sizes to embrace new business models that focus on outsourcing of various regulatory activities to reduce the pressure on their in-house team.

Outsourcing to India, China and other countries with cheap labour can commonly help companies realize cost savings of 30-60%. Other considered drivers for outsourcing regulatory activities include: flexibility, risk and security, regulatory impact, timely market approvals, Embassy Attestation, increased process speed, reducing time constraints in-house resources, NOC for Import and gaining access to broad global expertise and experience.

Pharma Regulatory Affair sactivities can range from simple tasks to very complex projects involving detailed consultation with relevant regulatory bodies and/or concerned health agencies. Successful outsourcing lies in finding a partner that is able to understand and adapt to an organization's needs and goals, while performing the functions efficiently and in a timely manner. The following factors play important roles in selecting a partner for outsourcing: experience, flexibility, effective communication, confidentiality, infrastructure, technology, resources, and quality of services delivered, cost benefit, accountability and geographic location/competencies.

Career Option: a Pharmacist

A pharmacist is a professional responsible for dispensing medications and handling prescriptions.  The role of the pharmacist is as important as that of any other medical professional.  The relationship that pharmacist's share with their patients is an important part of the care-giving circle. That relationship ensures that patients take their medications as prescribed so they may enjoy healthy lives.

To become a pharmacist, an individual must attend a 4-year bachelors program and complete a set of additional Written Confirmation to in order to receive their Doctorate in Pharmacology or PharmD degree.  An individual who desires to become a pharmacist must be strong in science and math as a lot of their certification is based on a study of chemistry, pharmacology, anatomy and physiology.  Although pharmacists do not operate on patients, they must have an understanding about how the body works and the basic chemical make-up of the human body.

Pharmacists are board certified practitioners who must pass a rigorous licensing examination in order to be able to practice.  Once these requirements have been met, a pharmacist begins practicing their profession.  Pharmacists are licensed by the state in which they do business, but are subject to both state and federal laws with respect to the dispensing medication, which is why they require Embassy attestation.

If you are planning a career as a pharmacist, you should spend some time at your local pharmacy and get a feel for the type of work that goes on from day to day.  If you are old enough, you may consider a summer position in the pharmacy as a way to gain a first-had perspective.  You should also take care to make sure that your chemistry and mathematical skills are very good and so is your knowledge about special documents like Form-41, Pharma regulatory Affairs,FSSAI, etc.

Pharmacy - A Lucrative Career Option

Pharma regulatory affairs professionals play an essential role in ensuring all pharmaceutical products comply with regulations governing the industry.

Those working in pharma regulatory affairs jobs not only work in the initial application phase for a new or generic drug, but also in the licensing and marketing stages – making sure all operations and products meet required safety and efficacy standards.

Professionals must combine knowledge of the business, legal and pharmaceutical industries to determine if regulations are being followed and in many cases form the link between pharma companies and regulatory authorities, such as the Food and Drugs Agency (FDA), FSSAI Consultant in India and the European Union.

There are different types of education a student can choose from, depending on their interest and skills. Students can start from Diploma to PhDs.

Students find employment in the following industries/sectors:-Drugs, Pharmaceuticals & Bio-pharma, Medical devices & equipment manufacturing, Cosmetics & Perfumes, Regulatory Affairs (Food & Drug Control Administration appointed by the government and Regulatory Affairs Depts., in companies), Patents, trademarks and IPR (Documentation department in government and private companies), Pharma journalism (Media editorial team), Blood banks, FSSAI,Consultancies - offering varied services. (Regulatory affairs, documentation, research, manufacturing, survey and analysis, information retrieval, data management, turn key projects etc.)

Opportunities for regulatory affairs consultants offer professionals the chance to work in a number of fields, which requires high levels of knowledge of multiple industries.

Jobs in pharma regulatory affairs generally require a background in the applicable industry, business knowledge, great oral and written communication, good attention to detail and strong IT skills.

Importance of Regulation In Pharma Industry

Today, Administrative Issues is an element specialty unit that works with a centre to get items to the business sector with monetarily practical mark at all possible time and costs. In perspective of the expanding worldwide aggressiveness among pharmaceutical organizations, the way to achievement lies in getting auspicious promoting approval from the Administrative Issues of the area where the medication is to be sold. Different Drug Registration Consultants are included in managing medications inside their business sector. 

DCGIConsultant in Delhi/India is one such agency which is involved in regulating drugs. Within Central Drugs Standard Control Organization, the Drug Controller General of India (DCGI) regulates pharmaceutical and medical devices, under the gamut of Ministry of Health and Family. Patent expiries, tightening healthcare budgets and a stricter regulatory climate are the major challenges to the pharmaceutical industry. Many companies are in a race to place their new products in the world market and to gain market share and increase earnings.

In such a scenario, a little deferin gaining market access meansenormous misfortunein terms of market share and revenue generated. The keys to success for pharmaceutical companies lie in obtaining timely marketing approval from regulators. So, to obtain timely marketing approval, companies can either strengthen their regulatory department or outsource the same to regulatory affairs consulting firm, like DCGI/CDSCO Approved in India. 

One cannot deny the fact that clinical trial is the basis for introducing better drugs, medical practices, and devices. The fact that it involves law and ethics makes it a challenge for those framing the legal provisions