KPC Group Chairman Kali P Choudhuri

Real Estate & Health Care Industry King- Kali P. Choudhuri

Kali Pradip Choudhury is the chairman and founder for of the KPC group and also an orthopedic surgeon. He belongs from a well know family the Choudhury bari from Sylhet, Bangladesh. His wife’s name is “Shunanda”, and they have one daughter and one son.

Health Care and Real Estate Industry King Dr. Kali Pradeep Choudhuri

Kali p. Choudhuri completed his MBBS from Kolkata and the studied in Malaysia, England, Canada and United States.because of Dr. Kali P. Chaudhuri’s extraordinary vision and acute entrepreneurship and hard work the KPC Group has reached an unprecedented level of success. Because of his gentle credit maintains a very modest attitude, makes himself accessible to friends and countrymen and retains great pride in his Bengali Heritage. He does not dwell on his success; he’s far from it. He prefers to maintain a low profile.

Here is some kali p Choudhury’s medical profession achievement:

§ Certified by the American Board of Orthopaedic Surgeons.
§ Fellow member of the American Academy of Orthopaedic Surgeons.
§ Fellow member of the American College of Surgeons.
§ Fellow member of the International College of Surgeons.
§ A faculty member of the prestigious Loma Linda University Medical School,        California, U.S.A.
§ Chairman, Department of Surgery, Hemet Valley Medical Centre, Inc.
§ Chairman, Orthopaedic Department, Hemet Community Medical Group, Inc.
§ Chairman, Orthopaedic Department, APEX Healthcare Medical Centre, Inc.

Kali_Chaudhuri_Hosts_Bangladesh

The KPC Group is engaged in many businesses around the world serving diverse industries such as healthcare services and facilities, pharmaceutical, biotechnology, education, real estate, infrastructure development, agriculture, architecture and engineering, alternative energy, waste management, travel services, and information technology. All these businesses are doing really good all over the world. His success as an Orthopaedic surgeon and Heath Care Businessmen, developer, political adviser, and Philanthropist make him a superlative choice for the ‘Man of The Year’.

Kali P. Choudhuri achieved success in many businesses while enhancing his footprint in healthcare services. In the last four months of 2010, Dr. Kali Choudhury and his Group acquire $70 million in four hospitals in California. In addition, Dr. Kali Chaudhuri successfully acquired two hospitals: Hemet Valley Medical Centre and Menifee Valley Medical Centre for $172 million. His latest hospital acquisition includes Victor Valley Community Hospital in Victorville, California.

He has been chief of staff and currently chief of the Orthopaedics department at Hemet Valley Medical Centre. He has built a large practice and has several other Orthopaedic Surgeons working for him. Dr. Kali Chaudhuri’s practice continues to grow to add more surgeons; as a result, a network covering the Inland Empire of Southern California. Dr. Choudhuri’s personal practice involves mainly total joint replacements. His Patients usually come from the local area, other parts of California, the U.S.A., and overseas, especially England, Canada, The Middle East, India, and Bangladesh.

kpc-medical-college-and-hospital

In the determination of developing a fully integrated healthcare delivery system; Dr. Kali Chaudhuri is a major shareholder in the network of surgery-centers and medical office complexes. He is also the Co-Founder and major shareholder of Southland Healthcare, which is one of the largest physician-owned Health Care providers in Southern California. Dr. Kali Chaudhuri is also following the process of integrating with a major Health Care network which will cover more than 250,000 Lives and has contracts with more than 250 primary care and 750 specialist physicians; as a result, the organizations would be one of the largest physicians owned and physician operated networks in the entire county.

Kali-Chaudhuri-KPC-Group-9-KPC

In the real estate business, Dr. Kali Chaudhuri has enhanced his footprints over the last several years. The KPC Group has a contract sign with the prestigious “ City of Corona Redevelopment” project, which is worth over $1.8 billion dollars over a period of several years. The KPC Group has built the multi-million dollar high profile 300,000 SF commercial complex in Corona, California and named it KPC Summit. In addition, Dr. Chaudhuri and his Group are currently engaged in the development and construction of more than 3.3 million sq. ft. of commercial real estate comprising of hotels, resorts, apartments, old age homes, and educational institutions.

kpc group head office

Dr. Chaudhuri is also determined to establish a modern hospital in Calcutta, emphasizing Orthopaedics and linked the projects to the O.S.C. network of centers in the United States. For this cause, he has bought land in the Eastern-bypass area in Calcutta and has received tremendous support from the government in West Bengal – in particular, the Honourable Chief Minister. He currently has two major projects Kali-Ka Prasad Charitable Hospital; established by Dr. Chaudhuri’s Great Grandfather in 1911 in Sylhet, Bangladesh, which is still functioning but she is in need of modernization. Dr. Chaudhuri is in the process of negotiating with the Bangladesh Government and has extended a commitment of one crores rupees for this purpose.

In 2003, Dr. Kali Chaudhuri had successfully established the first private medical school in West Bengal, India. On a sprawling 25 acres state-of-the-art campus with more than 1.8 million sq. ft. of construction, the KPC Medical College & Hospital, Shova Rani Nursing College and Paramedical College provide health and educational services to millions of Indians residing in the city of Kolkata. Kali P. Chaudhuri will discuss his organizations’ partnership with the Swiss company;  Protek AG – in the aim Corporation for pursuing a joint venture in India to manufacture Orthopaedics Implants and other products.
In April 2010, The KPC Group’s pharmaceutical company, “Chemgen Pharma International” partnered with Ferrer Group based in Barcelona, Spain to develop The KPC-Ferrer Institute for Infectious and Tropical Diseases.

The collaboration with Ferrer will combine the expertise of the two companies in the design of chemical compounds for developing anti-infective drugs. Also in 2010, Chemgen Pharma International entered into an agreement with Orthopaedic technique K.G. in Germany to develop Ortho-Chemgen; a multi-million dollar company with bases in India and Germany.
Dr. Kali Chaudhuri and his Group are also involved in the Information Technology and Architectural/Engineering/Construction sector.

In 2005, his Group created DowcoMAX Services to provide automated structural steel facilities to the worldwide steel market. DowcoMAX contributed to high-profile projects such as the Freedom Tower in New York City, the Goldman Sachs World Headquarters in New York and many others including Oil and Gas refineries throughout the world. In 2011, Dr. Kali Chaudhuri acquired DowcoMAX by enhancing his ownership position from 40% to 100% and renamed it ITeMAX Engineering Services.

Not only this Dr. Kali Chaudhuri also involved with the political arena as an officer and a member of several prestigious Republican Party organizations on a local and national scale. Recently, the governor of California, Pete Wilson, and his wife visited Dr. Chaudhuri’s residence in Hemet and personally thanked him for his community work and presented him with the Golden Bear of California.

Dr. kali p choudhuri family

Dr. Kali Chaudhuri is currently Co-Convener and Co-Sponsor in Riverside County of Mr. Wilson’s current Presidential campaign drive. Dr. Kali Chaudhuri is a driven leader who has derived his inspiration to build his dream from South Asian traditional culture, heritage, and values.

Active Pharmaceutical Ingredients database

Active Pharmaceutical Ingredients-(API) 2020

ACTIVE PHARMACEUTICAL INGREDIENTS (API) 2020

Definition

Active Pharmaceutical Ingredients is the term used to allude to the organically active part of a medication product (for example tablet, case). For instance, an active fixing to calm agony is incorporated into a painkiller. This is called Active Pharmaceutical Ingredients (API). A little measure of the app has an impact, so just a small piece of the Active Pharmaceutical Ingredients (API) is contained in the medication. You will discover the name and measure of the Active Pharmaceutical Ingredients (API) contained in the prescription on the bundle of OTC (over-the-counter) drugs.

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Active Pharmaceutical Ingredients Starting Material 2020

A crude material, halfway, or an Active Pharmaceutical Ingredient (API) that is utilized in the creation of another Active Pharmaceutical Ingredient and that is joined as a noteworthy basic piece into the structure of the Active Pharmaceutical Ingredients (API). An Active Pharmaceutical Ingredient (API) Starting Material can be an article of business, a material obtained from at least one provider under contract or business assertion, or created in-house. Programming interface Starting Materials are typical of characterized substance properties and structure.

Reference: Manufacturing, Processing, or Holding Active Pharmaceutical Ingredients FDA Guidance. This segment gives general and basic rules for choosing Active Pharmaceutical Ingredients (API)s reasonable to transdermal conveyance utilizing topical plans.

Active Pharmaceutical Ingredients (apis)

GMP for Active Pharmaceutical Ingredients Manufacturing 2020

Administrative Applicability

Inside the world network, materials may shift as to their legitimate characterization as Active Pharmaceutical Ingredients (API). At the point when a material is delegated an Active Pharmaceutical Ingredients (API) in the area or nation in which it is produced or utilized in a medicate item, it ought to be fabricated in this direction.

Scope

This direction applies to the assembling of Active Pharmaceutical Ingredients (API)s for use in human medication (restorative) items. It applies to the assembling of sterile Active Pharmaceutical Ingredients (API) just up to the indicate promptly earlier the active Pharmaceutical Ingredients being rendered sterile. The cleansing and aseptic preparing of sterile Active Pharmaceutical Ingredients are not secured by this direction, yet ought to be performed as per GMP directions for medication (restorative) items as characterized by neighborhood specialists.

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Obligations of the Quality Unit(s) 2020

The principal duties of the free quality unit(s) ought not to be assigned. These obligations ought to be depicted recorded as a hard copy and ought to incorporate, yet not really be constrained to the accompanying:

  1. Discharging or dismissing all Active Pharmaceutical Ingredients (API)s. Discharging or dismissing intermediates for use outside the control of the assembling organization
  2. Building up a framework to discharge or reject crude materials, intermediates, bundling, what’s more, marking materials
  3. Checking on finished clump creation and lab control records of basic process ventures before the arrival of the Active Pharmaceutical Ingredients (API) for dispersion
  4. Ensuring that basic deviations are explored and settled
  5. Supporting all determinations and ace creation guidelines
  6. Supporting all systems influencing the nature of intermediates or Active Pharmaceutical Ingredients
  7. Ensuring that inward reviews (self-examinations) are performed
  8. Favoring middle of the road and Active Pharmaceutical Ingredients (API) contract makers
  9. Favoring changes that possibly influence transitional or Active Pharmaceutical Ingredients (API) quality
  10. Investigating and supporting approval conventions and reports

 

Inside Audits (Self Inspection) 2020

To check consistency with the standards of GMP for Active Pharmaceutical Ingredients (API)s, normal interior reviews ought to be performed as per an endorsed timetable.

Review discoveries and remedial activities ought to be reported and conveyed to the consideration of mindful administration of the firm. Concurred remedial activities ought to be finished in an opportune what’s the more, powerful way.

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Item Quality Review

Customary quality-audits of Active Pharmaceutical Ingredients (API) ought to be directed with the target of confirming the consistency of the procedure. Such surveys ought to ordinarily be led and reported every year and ought to incorporate at any rate the accompanying:

  • A survey of basic in-process control and basic Active Pharmaceutical Ingredients (API) test results
  • A survey of all clumps that neglected to meet set up specification(s)
  • A survey of every single basic deviation or nonconformances and related examinations
  • A survey of any progressions did to the procedures or systematic strategies;
  • An audit of the consequences of the solidness checking program.
  • An audit of all quality-related returns, protests, and reviews
  • An audit of the sufficiency of remedial activities

The consequences of this survey ought to be assessed and an appraisal made of whether the restorative activity or any revalidation ought to be attempted. Explanations behind such restorative activity ought to be recorded. Concurred restorative activities ought to be finished in an auspicious and powerful way.

Personal Hygiene

Personnel should wear clean attire reasonable for the assembling action with which they are included and these garments ought to be changed, when suitable. Extra defensive attire, for example, head, face, hand, and arm covers, ought to be worn, when vital, to ensure intermediates and Active Pharmaceutical Ingredients (API)s from sullying. The workforce ought to maintain a strategic distance from direct contact with intermediates or Active Pharmaceutical Ingredients (API)s.

gmp of Active Pharmaceutical Ingredients (API) Unmarinero

Active Pharmaceutical Ingredients (API) Buildings And Facilities 2020

Plan and Construction

Buildings and facilities utilized in the production of intermediates and Active Pharmaceutical Ingredients (API) ought to be found, planned, and built to encourage cleaning, upkeep, and tasks as suitable to the type and phase of assembling.

There ought to be characterized zones or other control frameworks for the accompanying exercises:

  • Receipt, recognizable proof, testing, and isolate of approaching materials, pending discharge or dismissal
  • Quarantine before discharge or dismissal of intermediates and Active Pharmaceutical Ingredients (API)s
  • The sampling of intermediates and Active Pharmaceutical Ingredients (API)s
  • Holding rejected materials before further demeanor
  • Storage of discharged materials

Utilities

All utilities that could influence item quality (e.g., steam, gas, packed air, warming, ventilation, and cooling) ought to be qualified and fittingly checked and the activity ought to be taken when limits are surpassed. Illustrations for these utility frameworks ought to be accessible. Sufficient ventilation, air filtration, and fumes frameworks ought to be given, where fitting.

These frameworks ought to be structured and developed to limit the dangers of sullying and cross-contamination and ought to incorporate gear for control of pneumatic force.

  • Cleaning plans, including, where fitting, disinfecting plans
  • Instructions for the security of clean gear from pollution before use

Calibration

Control, gauging, estimating, checking, and testing hardware basic for guaranteeing the quality of intermediates or Active Pharmaceutical Ingredients (API) ought to be adjusted by composed techniques and a setup plan.

Gear adjustments ought to be performed utilizing gauges discernible to affirmed guidelines, on the off chance that they exist. Records of these adjustments ought to be kept up. The present alignment status of basic gear ought to be known and certain.

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Active Pharmaceutical Ingredients (API) Documentation & Records 2020

Documentation System and Specifications

All reports identified with the assembling of intermediates or Active Pharmaceutical Ingredients (API) ought to be readied, audited, affirmed, and dispersed by composed systems. Such records can be in paper or electronic structure.

Equipment Cleaning and Use Record

Records of significant hardware use, cleaning, sanitation, as well as sanitization and upkeep should demonstrate the date, time (if proper), item, and the cluster number of each group prepared in the hardware and the individual who played out the cleaning and upkeep. Records of Raw Materials, Intermediates, Active Pharmaceutical Ingredients (API) Labeling, and Packaging Materials Records ought to be kept up including the accompanying:

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Active Pharmaceutical Ingredients (API) Materials Management 2020

General Controls

There ought to be composed systems portraying the receipt, distinguishing proof, isolate, capacity, taking care of, inspecting, testing, and endorsement or dismissal of materials. Producers of intermediates and additionally Active Pharmaceutical Ingredients (API) ought to have a framework for assessing the providers of basic materials.

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Active Pharmaceutical Ingredients (API) Production and In-process Controls 2020

Production Operations

Raw materials for middle and Active Pharmaceutical Ingredients (API) assembling ought to be gauged or estimated under fitting conditions that don’t influence their appropriateness for use. Gauging and estimating gadgets should be of appropriate precision for the planned use.

Time Limits

In the event that time limits are indicated in the ace creation guidance (see 6.40), these time limits ought to be met to guarantee the nature of intermediates and Active Pharmaceutical Ingredients (API)s. Deviations ought to be archived also, assessed. Time breaking points might be wrong when preparing to objective esteem (e.g., pH modification, hydrogenation, drying to foreordained. )

In-process Sampling and Controls

Composed strategies ought to be built up to screen the advancement and control the execution of preparing steps that reason fluctuation in the quality attributes of intermediates and Active Pharmaceutical Ingredients (API)s. In-process controls and their acknowledgment criteria ought to be characterized dependent on the data picked up amid the formative stage or from verifiable information.

Contamination Control

Lingering materials can be persisted into progressive bunches of a similar middle of the road or Active Pharmaceutical Ingredients (API) if there is sufficient control. Models incorporate buildup clinging to the mass of a micronized, leftover layer of soggy precious stones staying in an axis bowl after release, and deficient release of liquids or precious stones from a preparing endless supply of the material to the following venture all the while.

Packaging and Identification Labeling of Active Pharmaceutical Ingredients (API) and Intermediates 2020

Packaging Materials

Compartments ought to give satisfactory assurance against decay or pollution of the middle of the road or Active Pharmaceutical Ingredients (API) that may happen amid transportation and prescribed stockpiling.

Compartments ought to be perfect and, were demonstrated by the idea of the middle of the road or Active Pharmaceutical Ingredients (API), purified to guarantee that they are reasonable for their planned use. These compartments ought not to be responsive, added substance, or absorptive in order to change the nature of the middle of the road or Active Pharmaceutical Ingredients (API) past the indicated limits.

Lebel Issuance and Control

Access to the name stockpiling zones ought to be restricted to the approved workforce.

Storage and Distribution of Active Pharmaceutical Ingredients (API) 2020

Warehousing Procedures

Facilities ought to be accessible for the capacity of all materials under fitting conditions (e.g., controlled temperature and stickiness when fundamental).

Distribution Procedures

Active Pharmaceutical Ingredients (API)s and intermediates should just be discharged for conveyance to outsiders after they have been discharged by the quality unit(s). Active Pharmaceutical Ingredients (API)s and intermediates can be exchanged under isolate to another unit under the organization’s control when approved by the quality unit.

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Active Pharmaceutical Ingredients (API) Laboratory Controls 2020

Testing of Intermediates Active Pharmaceutical Ingredients (API)

For each clump of the middle of the road and ACTIVE PHARMACEUTICAL INGREDIENTS (API), suitable research center tests ought to be directed to decide conformance to details.

Stability Monitoring of Active Pharmaceutical Ingredients (API)

An archived, on-going testing project ought to be set up to screen the steadiness attributes of Active Pharmaceutical Ingredients (API)s, and the outcomes ought to be utilized to affirm proper capacity conditions furthermore, retest or expiry dates.

Expiry and Retest Dating

At the point when a transitional is planned to be exchanged outside the control of the maker’s material administration framework and an expiry or retest date is appointed, supporting dependability data ought to be accessible.

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Active Pharmaceutical Ingredients (API) Validation 2020

Validation Policy

The organization’s general strategy, goals, and way to deal with approval, including the approval of generation forms, cleaning techniques, systematic strategies, in-process control test techniques, automated frameworks, and people in charge of configuration, survey, endorsement, and documentation of every approval stage, ought to be archived.

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Active Pharmaceutical Ingredients (API) Rejection and Re-use of Materials 2020

Rejection

Intermediates and Active Pharmaceutical Ingredients(API)s neglecting to meet set up details ought to be recognized accordingly and isolated. These intermediates or Active Pharmaceutical Ingredients (API)s can be reprocessed or improved as depicted underneath. The last demeanor of rejected materials ought to be recorded.

Reprocessing

Presenting a transitional or Active Pharmaceutical Ingredients (API), including one that does not fit in with norms or determinations, once more into the procedure and reprocessing by rehashing a crystallization step or other suitable substance or physical control steps.

active pharmaceutical ingredients

 

Active Pharmaceutical Ingredients (API)s For Use in Clinical Trials 2020

The controls utilized in the assembling of Active Pharmaceutical Ingredients (API)s for use in clinical preliminaries ought to be steady with the phase of the advancement of the medication item fusing the Active Pharmaceutical Ingredients (API). Procedure and test methods ought to be adaptable to accommodate changes as information of the procedure increments and clinical trials or testings of a medication item advances from pre-clinical stages through clinical stages.

During all periods of clinical improvement, including the utilization of little-scale offices or research centers to make bunches of Active Pharmaceutical Ingredients (API)s for use in clinical preliminaries, systems ought to be in the spot to guarantee that hardware is adjusted, clean, and reasonable for its proposed use.

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At The End

The nature of Active Pharmaceutical Ingredients (API)s significantly affects the adequacy and security of drugs. Inadequately fabricated or traded off Active Pharmaceutical Ingredients (API)s have been associated with significant issues, for example, diseases and even passing.

Indeed, even on account of redistributing, Active Pharmaceutical Ingredients (API)s are liable to stringent guidelines and oversight from the nation they are transported to. For instance, Active Pharmaceutical Ingredients (API) fabricating plants abroad still experience an examination by the U.S. Sustenance and Drug Administration.

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