GerdLi: New Supplement for Heartburn Was Made by a Physician Who Sought Natural Heartburn Relief

GerdLi: New Supplement for Heartburn Was Made by a Physician Who Sought Natural Heartburn Relief

November 1, 2022 Eric Jones 0

GerdLi: New Supplement for Heartburn Was Made by a Physician Who Sought Natural Heartburn ReliefGerdLi: New Supplement for Heartburn Was Made by a Physician Who Sought Natural Heartburn ReliefAfter developing severe esophagitis and being prescribed life-long medications, Jimmy Minhas, a doctor and founder of GerdLi, researched and created the world’s first natural supplement to relieve heartburn and acid reflux.

SEATTLE – November 1, 2022 – (Newswire.com)

Physician-engineered GerdLi is the natural answer for people who live with acid reflux and heartburn. It’s a premium-formulated antacid that maintains gut health and allows one to get back to eating the foods one loves. For those who hate to swallow pills, GerdLi comes as a small, easy-to-swallow capsule.

People that suffer from gastroesophageal reflux disease (GERD) are left to take prescription medications and must reduce or eliminate eating spicy foods, acrid vegetables, fatty, fried foods, fruit juices, wine, coffee and soda. Even large meals or eating before bedtime can cause uncomfortable acid reflux symptoms and, at times, damage to the esophagus.

GerdLi contains D-limonene, derived from the rinds of citrus fruits such as oranges, mandarins, lemons, limes and grapefruits and works in several ways to help with GERD.

  • D-limonene decreases stomach acid
  • It relieves symptoms of GERD, including indigestion, sour taste, regurgitation and bloating
  • GerdLi is made with non-GMO ingredients, is vegan, gluten-free and has no artificial flavors or fillers

So many products on the market aiming to combat GERD and acid reflux, but GerdLi is by far the best remedy I’ve used. GerdLi offers great relief and the fact that it’s created by doctors makes it stand out even more.” MK, Happy Customer

GerdLi was developed over three years, and after three months of trials and testing, half the participants found improvement in their GERD symptoms. GerdLi may work as soon as one week and averages 2-4 weeks for relief of acid reflux symptoms. One study showed 72% of the participants experienced improvement within the 2-4 week period. 

Although GerdLi is proven to alleviate heartburn and symptoms of GERD, lifestyle changes are just as crucial to a successful acid reflux regimen. GerdLi is meant to complement healthy lifestyle habits allowing patients to choose a natural way to relieve acid reflux and heartburn. Improved health includes staying active, eating clean foods and staying hydrated by drinking lots of water throughout the day. 

GerdLi is manufactured in a special FDA-registered facility, ensuring it’s a safe supplement made with the highest quality ingredients. High-potency D-limonene is carefully sourced to be sure each bottle of GerdLi delivers the most effective results for reducing acid reflux. It works as an alkaline in the stomach to reduce acid, and its name is derived from lemon rinds, which have the highest concentration of limonene.

Once D-limonene is taken, it’s rapidly absorbed in the gastrointestinal tract and distributed into tissue. GerdLi reduces heartburn and reflux symptoms and may help some people reduce the amount of prescription medication they take. 

The mission at GerdLi is to help people suffering from acid reflux while offering them an alternative to prescription medications that often cause side effects. GerdLi also cares about creating a healthier world, donating part of its proceeds to support the Esophageal Cancer Society. 

Contact Information:

Matt Kane

Media manager
[email protected]

680 850 3345

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GerdLi: New Supplement for Heartburn Was Made by a Physician Who Sought Natural Heartburn Relief

New Jersey Podiatrist Teams with Ankle & Foot Centers of America

New Jersey Podiatrist Teams with Ankle & Foot Centers of America

November 1, 2022 Editor 0

New Jersey Podiatrist Teams with Ankle & Foot Centers of AmericaNew Jersey Podiatrist Teams with Ankle & Foot Centers of AmericaLeading podiatrist in Wayne, New Jersey, partners with the Ankle & Foot Centers of America, the nation’s leading group of foot and ankle surgeons. This relationship allows doctors to dedicate their time to treating patients instead of administrating a podiatry practice.

WAYNE, N.J. – November 1, 2022 – (Newswire.com)

Renown New Jersey podiatrist Lindsey Calligaro, DPM, of Wayne Foot & Ankle Center has recently teamed with Ankle & Foot Centers of America, the market leader in physician practice management and process improvement, to better serve patients. Wayne Foot & Ankle Center has been providing the highest-quality care to patients for over 40 years, and is dedicated to improving the lives of people in the northern NJ community.

Dr. Lindsey Calligaro earned her Doctor of Podiatric Medicine from the New York College of Podiatric Medicine in 2011 and attended a comprehensive three (3) year residency in Scranton, Pennsylvania with Dr. Guido LaPorta. Dr. Calligaro served as Chief Fellow during her fellowship in Baltimore, Maryland, at the Rubin Institute for Advanced Orthopedics/International Center for Limb Lengthening. Dr. Calligaro’s training specialized in complex foot and ankle deformity correction and pediatric deformity correction. Dr. Calligaro treats a variety of foot and ankle problems, including bunions, heel pain, trauma, and flatfeet. She also specializes in all aspects of pediatric foot and ankle deformity correction with a special interest in clubfoot. Helping to serve the needs of patients is what brought Dr. Calligaro to podiatry, and it is what motivates her to provide the best care possible every day.

Teaming with Ankle & Foot Centers of America allows physicians like Dr. Calligaro to do what they do best, take care of patients. With Ankle and Foot Centers of America, Dr. Calligaro is now able to benefit from the most advanced software, reporting, and office support in the industry. As healthcare becomes more complicated with technology and regulation, physicians must rely on expert support.

Incorporating the central scheduling team and call center from Ankle and Foot Centers of America allows patients to make appointments with greater ease with this Wayne, NJ, Podiatrist. Whether booking online or over the phone, patients can now expect to have a more streamlined experience. Additionally, Ankle and Foot Centers of America incorporates advanced network safeguards to better protect patient data and provides new training for staff on the latest advances and changes in healthcare.

With a shared commitment to excellence and dedication to patient well-being, Dr. Calligaro and the team at Ankle and Foot Centers of America look forward to treating the foot and ankle needs of patients in north New Jersey.

About Ankle & Foot Centers of America – Founded in Atlanta over 30 years ago, Ankle & Foot Centers of America is dedicated to providing patients with top-tier service and support through best-in-class technology and processes so that physicians can optimize patient outcomes and satisfaction.

Contact Information:

Alexis Pickford

Marketing Representative

678-561-9000

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Gb Sciences Co-Publishes Study Demonstrating Anti-Inflammatory Properties of Cannabis Ingredients

Gb Sciences Co-Publishes Study Demonstrating Anti-Inflammatory Properties of Cannabis Ingredients

November 1, 2022 Eric Jones 0

Gb Sciences Co-Publishes Study Demonstrating Anti-Inflammatory Properties of Cannabis IngredientsGb Sciences Co-Publishes Study Demonstrating Anti-Inflammatory Properties of Cannabis IngredientsAs published in the journal Food and Chemical Toxicology, the biopharmaceutical drug development firm’s sponsored research used co-cultured human, primary immune cells as a model to evaluate the ability of selected Cannabis constituents to decrease inflammation.

LAS VEGAS – November 1, 2022 – (Newswire.com)

Gb Sciences, Inc. (OTCQB:GBLX), a leading plant-inspired, biopharmaceutical research and drug development company, has co-published a study in the journal Food and Chemical Toxicology that demonstrates the potential of selected cannabinoids and terpenes to reduce inflammation. Finding Cannabis compounds with anti-inflammatory properties may be useful in decreasing inflammation associated with a wide range of serious human disorders, and these Cannabis compounds potentially have more favorable side effect profiles than NSAIDs (Non-Steroidal Anti-Inflammatory Drugs), which currently lead the anti-inflammatory market based on sales. Largely because of the increasing prevalence of chronic and auto-immune inflammatory disorders, the market for anti-inflammatory therapies is expected to grow to $191.42 billion by 2027.

“We believe that this is the first demonstration of the anti-inflammatory potential of some very potent minor cannabinoids and terpenes derived from Cannabis,” said Dr. Andrea Small-Howard, President, Chief Science Officer, and Director of Gb Sciences. “The identification of cell type-specific immune modulating effects by different individual cannabinoids and terpenes was an important first step in designing our novel anti-inflammatory therapies. The results from our second study on the anti-inflammatory effects of proprietary mixtures of these ingredients will be published subsequently with our collaborators at Michigan State University and Chaminade University.”

Gb Sciences selected the specific Cannabis constituents for this study based on their prior activity within chemovar studies. To determine whether these cannabinoids and terpenes could reduce inflammation, Gb Sciences’ colleagues at Michigan State University tested the individual Cannabis constituents over a wide range of concentrations in human, primary immune cells in a co-culture system that mimics the complex interactions that regulate the human immune system. Three immune cell types were chosen as representatives within these native human immune cell mixtures based on their important roles in modulating the inflammatory cascade.

This study demonstrated that delta-9 tetrahydrocannabinol (THC) had the greatest effect on reducing inflammatory biomarkers and processes in all three immune cell types. Following THC, the greatest immune activity modulation was measured by cannabidivarin (CBDV), cannabigerol (CBG), cannabichromene (CBC), cannabinol (CBN), and lastly, cannabidiol (CBD) in decreasing order based on the number of statistically significant changes measured in inflammatory bioassays relative to the control. Some of these minor cannabinoids and the terpenes tested had very ‘selective’ anti-inflammatory effects, which targeted a single cell type and/or caused a change in only a single inflammatory bioassay.

This study entitled “Evaluation of the anti-inflammatory effects of selected cannabinoids and terpenes from Cannabis Sativa employing human primary leukocytes” was co-authored by Gb Sciences’ own President and Chief Science Officer, Andrea Small-Howard, and her collaborators Lance K. Blevins, Anthony P. Bach, Robert B. Crawford, Jiajun Zhou, Joseph E. Henriquez, Michael D. Rizzo, Sera Sermet, D.M. Isha Olive Khan, and Norbert Kaminski from Michigan State University (East Lansing, Michigan, USA) and Helen Turner from Chaminade University of Honolulu (Honolulu, Hawai’i, USA). The second part of this study measured the effects of proprietary mixtures of cannabinoids and terpenes on inflammation within this human, primary immune cell model, and this second study will be published next in collaboration with our colleagues at Michigan State University and Chaminade University.

To learn more about Gb Sciences, visit www.gbsciences.com.

About Gb Sciences and GbS Global Biopharma

Gb Sciences, Inc. is a plant-inspired, biopharmaceutical research and development company creating patented, disease-targeted formulations of cannabis- and other plant-inspired therapeutic mixtures for the prescription drug market through its Canadian subsidiary, GbS Global Biopharma, Inc. The ‘plant-inspired’ active ingredients in its therapeutic mixtures are synthetic homologues identical to the original plant compounds but produced under current Good Manufacturing Practices. Gb Sciences’ intellectual property portfolio contains six issued U.S. and three issued foreign patents, as well as 17 U.S. and 51 foreign patent-pending applications. In its drug development pipeline, Gb Sciences has five preclinical phase product development programs. Gb Sciences’ lead program for Parkinson’s disease is being prepared for a first-in-human clinical trial. Gb Sciences’ formulations for chronic pain, anxiety, and depression are currently in preclinical animal studies with researchers at the National Research Council of Canada. The company also received positive preclinical proof-of-concept data supporting its complex mixtures for the treatment of Cytokine Release Syndrome related to COVID-19, and its lead candidates will be optimized based on late-stage preclinical studies at Michigan State University. Gb Sciences’ productive research and development network includes distinguished universities, hospitals, and Contract Research Organizations. To learn more, visit www.gbsciences.com.

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Gb Sciences Co-Publishes Study Demonstrating Anti-Inflammatory Properties of Cannabis Ingredients

New CDMO Client, Quality Chemical Laboratories, Benefits From InstantGMP’s All-in-One Quality & Manufacturing System and Software Auditing for GMP Manufacturers

New CDMO Client, Quality Chemical Laboratories, Benefits From InstantGMP’s All-in-One Quality & Manufacturing System and Software Auditing for GMP Manufacturers

November 1, 2022 Editor 0

New CDMO Client, Quality Chemical Laboratories, Benefits From InstantGMP’s All-in-One Quality & Manufacturing System and Software Auditing for GMP Manufacturers

CARY, N.C. – November 1, 2022 – (Newswire.com)

InstantGMP, the originators of the all-in-one manufacturing and quality system, is proud to welcome a new contract development and manufacturing organization, Quality Chemical Laboratories (QCL), to its growing client base.

Quality Chemical Laboratories was founded in 1998 as a raw material testing laboratory and has continuously expanded capabilities and service offerings. For over 25 years, this leading CDMO has provided GMP-compliant formulation development and manufacturing services for the pharmaceutical industry. The company’s clients range from small start-up companies to some of the most prominent pharmaceutical corporations in the world.

As its client base continues to grow, Quality Chemical Laboratories recognized the importance of implementing a new software system to enhance its processes while gaining efficiency and maintaining GMP and FDA compliance.

QCL’s exhaustive search for a new software system led the company to the InstantGMP PRO system. While the software’s all-in-one capabilities impressed the QCL team, they required computer system validation to determine if the system:

  • Meets FDA Part 11 compliance.
  • Achieves its intended purpose by meeting user requirements.
  • Is free from any installation or performance issues that could negatively impact the integrity of the CDMO’s production cycles, raw materials or finished pharmaceutical products.

To ensure that the InstantGMP PRO system was validated, Quality Chemical Laboratories conducted an extensive software vendor audit. During the software vendor auditing process, QCL reviewed every piece of the software’s validation documentation and standard operating procedures (SOPs) via a virtual session with InstantGMP to confirm that InstantGMP PRO:

  • Is properly validated.
  • Vendor documentation can be appropriately leveraged to save QCL significant time and resources.
  • Functions accordingly and accurately.
  • Aligns with the information defined in the provided user requirement documentation.

After QCL reviewed all the respective documentation and asked any pertinent questions, it created and supplied a detailed audit report that identified topics that required further discussion and some minor issues that needed to be resolved. At the conclusion of the audit process, InstantGMP successfully satisfied Quality Chemical Laboratories’ requirements.

Not only did this process lead to a successful relationship, but it also provided the QCL team a better understanding of the software’s full capabilities. Additionally, the audit process offered InstantGMP an opportunity to address previously unidentified issues and further enhance the software with new features that best meet manufacturers’ needs.

InstantGMP is excited to provide Quality Chemical Laboratories with a validated all-in-one software system that truly meets its needs for improved processes and assured compliance. InstantGMP wishes them continued success in the contract formulation development and manufacturing industry and thanks them for helping InstantGMP enhance their software during the audit process.

To learn more about InstantGMP PRO‘s new features and software auditing processes for GMP manufacturers, contact us to schedule a demonstration.

Contact Information:

Robert Pochadt

Director of Sales

[email protected]

215-975-9660

Jeremy Hall

Technical Sales Manager

[email protected]

757-759-4500



Related Files
InstantGMP PRO for FDA Requlated Industries 4.22.pdf

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New CDMO Client, Quality Chemical Laboratories, Benefits From InstantGMP’s All-in-One Quality & Manufacturing System and Software Auditing for GMP Manufacturers