Non-invasive light-based techniques may improve detection of skin cancer, reveals study

A study conducted by Aston University researchers has demonstrated that the appearance of ageing skin looks noticeably different compared to younger skin, when examined under polarised laser light.

The scientists believe that their new finding could pave the way for new, non-invasive light-based techniques to detect diseases, including cancer, in older individuals.

This could significantly enhance early-stage treatment options for various skin conditions.

It has already been established that two classes of polarised, linearly and circularly, can detect changes in skin that aren’t visible to the human eye.

The new study indicates that the altered light scattering properties of ageing skin are largely due to changes in the skin’s texture, which are associated with the depletion of collagen fibres in the dermal layer.

The research was led by Igor Meglinski, professor in quantum biophotonics & biomedical engineering and conducted under his guidance with Dr Viktor Dremin from Aston University’s Institute of Photonic Technologies.

The paper “Incremental residual polarization caused by aging in human skin” will be published in the May 2024 edition of the Journal of Biomedical Optics.

The researchers analysed images of the middle fingers of 32 volunteers aged 22 to 76 to study skin aging.

They also used the Monte Carlo method, a mathematical technique, to represent the effects of light circulation within the human skin.

This technique was developed by Professor Meglinski in 2001.

Combined with the visual data from the images, this enabled the researchers to draw conclusions about the optical properties of ageing skin.

Professor Meglinski said: “Our research offers a comprehensive analysis of how aging affects human skin polarisation properties. This could be a stepping stone to developing non-invasive, light-based techniques for early detection of skin conditions, including cancer, in the elderly.”

The findings of the research could support the development of a method of skin analysis which doesn’t rely on the patient undergoing biopsies or surgery.

It could provide instant assessments of age-related skin changes that can be extended to monitor changes associated with the development of diabetes and other conditions.

Reference:

Viktor Dremin, Elena Zharkikh, Ivan Lopushenko, Zbignevs Marcinkevics, Alexander Bykov, Igor Meglinski. Incremental residual polarization caused by aging in human skin. Journal of Biomedical Optics, 2023; 29 (05) DOI: 10.1117/1.JBO.29.5.052912.

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Infusion of human apolipoprotein A1 fails to reduce cardiovascular events in acute MI patients: NEJM

A recent international clinical trial by C. Michael Gibson and colleagues investigated the efficacy of CSL112 (human Apolipoprotein A1) which helps in reducing the risk of recurrent cardiovascular events in patients who have experienced acute myocardial infarction. The findings were published in The New England Journal of Medicine  and highlight the potential of CSL112 to improve the patient outcomes following such critical cardiac events.

This double-blind, placebo-controlled trial enrolled a substantial group with a total of 18,219 patients who underwent acute myocardial infarction, multivessel coronary artery disease and additional cardiovascular risk factors. The participants were randomly assigned to receive either four weekly infusions of 6 grams of CSL112 or a matching placebo where the first infusion was administered within five days after the initial medical contact for the heart attack.

Despite the promising premise of CSL112, the results of the trial found that over the 90-day follow-up period, there was no significant difference observed between the CSL112 group and the placebo group in terms of the primary endpoint, which is a composite of myocardial infarction, stroke or death from cardiovascular causes. This lack of divergence persisted throughout the 180-day and 365-day follow-up periods as well.

Also, the data revealed that 4.8% of patients in the CSL112 group experienced primary endpoint events at 90 days when compared to the 5.2% in the placebo group. At 180 days, the rates were 6.9% against 7.6%, and at 365 days, 9.8% against 10.5%, respectively. It is important to note that the percentages of adverse events were comparable between the two groups, although an increased number of hypersensitivity events were reported in the CSL112 group.

This comprehensive investigation suggests that among patients with acute myocardial infarction, multivessel coronary artery disease and additional cardiovascular risk factors, the administration of four weekly infusions of CSL112 did not lower the risk of myocardial infarction, stroke or death from cardiovascular causes when compared to placebo over a 90-day period.

While these results may come as a setback for post-myocardial infarction care, it helps in understanding the complexities involved in addressing recurrent cardiovascular events. Further research and development efforts are warranted to explore alternative strategies or refine existing approaches to improve patient outcomes and reduce the burden of cardiovascular disease.

Reference:

Gibson, C. M., Duffy, D., Korjian, S., Bahit, M. C., Chi, G., Alexander, J. H., Lincoff, A. M., Heise, M., Tricoci, P., Deckelbaum, L. I., Mears, S. J., Nicolau, J. C., Lopes, R. D., Merkely, B., Lewis, B. S., Cornel, J. H., Trebacz, J., Parkhomenko, A., Libby, P., … Harrington, R. A. (2024). Apolipoprotein A1 Infusions and Cardiovascular Outcomes after Acute Myocardial Infarction. In New England Journal of Medicine. Massachusetts Medical Society. https://doi.org/10.1056/nejmoa2400969

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Hearing Loss Linked to Faster Brain Atrophy and Cognitive Decline in Older Adults: Study

Recent research has suggested a potential link between hearing loss and an increased risk of dementia. However, the underlying mechanisms and how they relate to neurodegeneration and cognitive decline remain unclear. A new study sheds light on these relationships and their impact on dementia risk. The study was published in the Journal Of Neurology Neurosurgery and Psychiatry. The study was conducted by Thomas D. and colleagues.

Hearing loss has been proposed as a modifiable risk factor for dementia, but the specific pathways involved are not well understood. This study aimed to investigate how hearing impairment relates to brain atrophy and cognitive decline, and whether pathological processes such as Alzheimer’s disease and cerebrovascular disease influence these relationships.

The study analyzed data from 287 adults born in the same week of 1946 who underwent baseline pure tone audiometry at an average age of 70.6 years. Participants also underwent two time point cognitive assessment and multimodal brain imaging with a mean interval of 2.4 years. Hearing impairment was defined as a pure tone average of greater than 25 decibels in the best hearing ear. Rates of change for whole brain, hippocampal, and ventricle volume were estimated from structural MRI. Cognitive function was assessed using the Pre-clinical Alzheimer’s Cognitive Composite. Regression models were used to evaluate the associations between baseline hearing impairment, brain atrophy, and cognitive decline, adjusting for confounding factors including β-amyloid deposition and white matter hyperintensity volume.

The key findings of the study were as follows:

  • Out of the 287 participants, 111 had hearing impairment.

  • Hearing impaired individuals had faster rates of whole brain atrophy compared to those with preserved hearing.

  • Worse hearing (higher pure tone average) predicted faster rates of hippocampal atrophy.

  • In participants with hearing impairment, faster rates of whole brain atrophy were associated with greater cognitive decline.

  • These relationships were independent of β-amyloid deposition and white matter hyperintensity volume, suggesting that hearing loss may influence dementia risk via distinct pathways.

The study suggests that hearing loss may contribute to dementia risk through pathways separate from those typically associated with Alzheimer’s and cerebrovascular disease. Understanding these pathways could lead to new strategies for dementia prevention and intervention in older adults with hearing impairment.

Reference:

Parker, T. D., Hardy, C., Keuss, S., Coath, W., Cash, D. M., Lu, K., Nicholas, J. M., James, S.-N., Sudre, C., Crutch, S., Bamiou, D.-E., Warren, J. D., Fox, N. C., Richards, M., & Schott, J. M. (2024). Peripheral hearing loss at age 70 predicts brain atrophy and associated cognitive change. Journal of Neurology, Neurosurgery, and Psychiatry, jnnp-2023-333101. https://doi.org/10.1136/jnnp-2023-333101

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Use of Low-Dose Colchicine Safe for Prevention of Coronary artery Disease, new Study Reveals

In a recent review, researchers have shed light on the safety profile of low-dose colchicine, offering reassuring evidence for its use in secondary prevention among patients with coronary artery disease. The study, drawing from a comprehensive analysis of contemporary systemic reviews, case reports, drug registries, and placebo-controlled trials, aims to inform healthcare professionals and patients about the absolute risks associated with continuous use of this medication.

The study results were published in the European Heart Journal. The FDA has recently granted approval for the use of low-dose colchicine (0.5 mg daily) in the secondary prevention of coronary disease, marking a significant milestone in clinical practice. A comprehensive State-of-the-Art Review was conducted to gather data from contemporary systemic reviews, case reports, drug registries, and placebo-controlled trials. This analysis aimed to assess the safety implications associated with the continuous administration of colchicine across various clinical contexts. The goal was to provide crucial insights to physicians, pharmacists, and patients regarding the absolute risks linked with the sustained use of low-dose colchicine, including its impact on individuals concurrently prescribed statin therapy.

Findings:


  • One of the key findings highlighted in the review is the overwhelmingly positive safety profile of low-dose colchicine.
  • According to the data collated, the most commonly reported side effect is mild diarrhea, typically occurring during the initiation phase of treatment and subsiding within a week for the vast majority of patients.
  • Crucially, the review found no significant adverse effects of low-dose colchicine on renal, liver, or cognitive function.
  • Furthermore, the medication does not appear to impact bleeding, wound healing, fertility, or pregnancy outcomes.
  • No evidence was found to suggest an increased risk of cancer, serious infection, or cause-specific mortality associated with its use.
  • Of particular interest is the investigation into potential interactions between low-dose colchicine and statin therapy, a commonly prescribed treatment for cardiovascular disease.
  • Contrary to concerns, the data indicate that patients concurrently taking statins do not face heightened risks of myelosuppression, myotoxicity, or serious drug interactions when prescribed low-dose colchicine.

The implications of these findings are profound for clinical practice. Physicians, pharmacists, and patients can now approach the use of low-dose colchicine with greater confidence, especially in the context of reducing cardiovascular risk among individuals with atherosclerosis. Importantly, the review suggests that when appropriately prescribed to patients without significant renal or hepatic impairment, the risks associated with continuous use of low-dose colchicine are minimal. This study marks a significant milestone in our understanding of low-dose colchicine, paving the way for its wider adoption in clinical practice as a safe and effective therapy for cardiovascular disease.

Further research: Nidorf, Stefan Mark et al. “Low-dose colchicine for atherosclerosis: long-term safety.” European heart journal, ehae208. 10 Apr. 2024, doi:10.1093/eurheartj/ehae208

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Evidence of lasting lung damage, impaired lung function found in TB patients even after successful treatment: Study

New research being presented at this year’s ESCMID Global Congress (formerly ECCMID) in Barcelona, Spain (27-30 April) has found compelling evidence that tuberculosis (TB) can have a lasting impact on the lungs of individuals who have been successfully treated for the disease.

TB survivors have smaller lungs with narrower airways and slower air flow, the analysis of data on tens of thousands of individuals from around the world found.

“This damage could have a profound effect on long-term health, reduce quality of life and affect ability to work and carry out day-to-day tasks,” says lead researcher Dr Sharenja Ratnakumar, of St George’s, University of London, London, UK. “And, with growing numbers of people being successfully treated for TB, the finding strongly indicates that post-TB lung disease is an under-recognised global challenge.”

TB can be cured with antibiotics and, worldwide, an estimated 155 million people are alive today as a result of successful diagnosis and treatment of the bacterial infection.

However, although significant progress has been made in combating TB in recent decades, the number of new diagnoses has increased since the COVID-19 pandemic. Some 7.5 million were diagnosed globally in 2022 – the highest number since monitoring began in 1995 and above the pre-Covid baseline of 7.1 million in 2019, according to WHO’s 2023 Global Tuberculosis Report.1

The burden is highest in sub-Saharan Africa and south east Asia but even low incidence countries such as the UK are seeing diagnoses increase. According to provisional data from the UK Health Security Agency, there were 4,850 new diagnoses in England in 2023. This is above pre-Covid levels and represents a rise of more than 10% on 2022, when there were 4,380 diagnoses.2

Previous research has found that between 18% and >80% of survivors will be left with lung damage3 that reduces their quality of life and life expectancy4 but data on the size and type of respiratory impairment is scarce. To find out more, Dr Ratnakumar and colleagues carried out a systematic review and meta-analysis of existing research on the topic.

The Medline, Embase and CINAHL databases were searched from 1/01/00 to 31/01/23 for studies that compared the lung function of individuals with a history of TB with that of healthy controls.

The meta-analysis included data on 75,631 individuals from 15 studies conducted in 17 countries with varying TB incidence and income levels.

The 7,377 TB survivors had an average age range of 11-65 years. Many of the studies were skewed towards a younger population (<50years) from mainly low- and middle-income countries.

Four measures of lung function were included in the analysis: forced expiratory volume in 1 second (FEV1, the volume of air can be forcefully exhaled in one second); forced vital capacity (FVC, the volume of air that can be forcefully exhaled in a single breath); FEV1/FVC ratio; FVC as a percentage of the predicted value (compares the volume to the average of a healthy person of the same age, sex and height).

The study, which was supported by the charity Breathing Matters, found that, compared to the healthy controls, the participants with prior TB had significantly lower results on all four measures of lung function, with FEV1 more affected than FVC.

Dr Ratnakumar says: “FEV1 was 230 millilitres lower compared to healthy controls and FVC was 140 millilitres lower. A decrease in FEV1 of 100 millilitres is considered clinically significant and is associated with an increased risk of cardiovascular and respiratory disease.”5

The results as a whole point to the TB survivors having smaller lungs (restrictive disease) and narrower airways with slower air flow (obstructive disease). This means that the breaths they take are smaller and take longer; breathing is less efficient and less able to respond to increased ventilatory demands such as during exercise.

Analysis of data from five of the studies showed the TB survivors to have 65% higher odds of airflow obstruction (AFO) than the healthy controls.

The results suggest TB can leave a lasting and widespread impact on the lungs, especially in terms of how the airways are structured. This valuable insight can help guide rehabilitation strategies and, in the longer term, aid in the development of new therapies, say the researchers.

Dr Ratnakumar explains: “Our results strongly indicate that post-tuberculosis lung disease is an under-recognised global challenge – and one that has significant implications for clinical practice and policy.

“The focus, until now, has been on the treatment of acute TB, but even when treatment is successful, individuals can be left with significant lung damage.

“This can cause breathlessness that can affect their ability to work and go about their day-to-day lives and reduces their quality of life.

“This legacy of TB has been overlooked for too long and it is vital it is recognised.

“With an estimated 74 million lives saved through tuberculosis treatment between 2000 and 2020 and a rising life expectancy, there is an urgent need for evidence-based recommendations on the diagnosis, treatment and management of post-tuberculosis lung disease.

“Our study also provides compelling evidence that the long-term care of individuals with post-tuberculosis lung disease should be an explicit component of the WHO’s End TB strategy.”

Tuberculosis can have a lasting impact on the lung health of individuals who have been successfully treated for the disease ESCMID Global (ECCMID 2024)

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Migraine History Linked to Persistent Dysphotopsia after Monofocal Lens Implantation, claims study

Dysphotopsia, characterized by the perception of visual disturbances such as glare or halos, is a common concern following cataract surgery with intraocular lens (IOL) implantation. While transient dysphotopsia often resolves spontaneously, persistent dysphotopsia can significantly impact patient satisfaction and quality of life.

Researchers have found in a new study that history of migraine was associated with increased dysphotopsia severity and decreased patient satisfaction following cataract surgery with intraocular lens (IOL) implantation.

The study published in the Canadian Journal Of Ophthalmology was conducted by Maggie J. and colleagues.

Previous studies have explored various factors contributing to dysphotopsia, including IOL design, pupil size, and optical properties. However, the role of neuroadaptation-related risk factors, such as migraine history, remains less understood. Migraine is known to involve neurovascular mechanisms that could influence visual perception and potentially exacerbate dysphotopsia symptoms.

In this retrospective cohort study, conducted at an academic institution and a private practice in Saint Louis, Missouri, researchers aimed to identify neuroadaptation-related risk factors for persistent positive dysphotopsia (>6 months) following monofocal lens implantation. Participants included adults who underwent cataract extraction with monofocal IOL implantation between January 2010 and April 2021. Exclusion criteria comprised dementia, visual pathway damage, and significant pathology causing photopsia.

The key findings of the study were as follows:

  • The study included 385 participants (385 eyes), of whom 66 experienced persistent dysphotopsia (58 positive), while 298 had none, and 21 had nonpersistent dysphotopsia.

  • Migraine prevalence was higher among individuals with dysphotopsia (21.2%) compared to those without (11.4%).

  • History of migraine was associated with an increase in Pseudophakic Dysphotopsia Questionnaire 6 (PDQ-6) score by 2.76 points (p = 0.006).

  • Six individuals in each group had Visual Aura Rating Scale (VARS) scores greater than zero.

  • The mean VARS score was significantly higher in the dysphotopsia group (0.48) compared to the non-dysphotopsia group (0.14) (p = 0.03).

  • Younger age, female sex, history of migraine, and higher VARS score were associated with lower satisfaction levels among participants with dysphotopsia.

The study findings suggest that a history of migraine is associated with increased severity of dysphotopsia and decreased patient satisfaction following monofocal lens implantation. These results underscore the importance of considering migraine history in patient selection and counseling to optimize surgical outcomes and enhance patient satisfaction. Further research with larger sample sizes is warranted to validate these findings and inform personalized approaches to cataract surgery.

Reference:

Xing, M. J., Moulin, T. A., Suresh, T., Gira, J. P., Sheybani, A., & Van Stavern, G. P. (2024). Migraine is a risk factor for pseudophakic positive dysphotopsia following monofocal lens implantation. Canadian Journal of Ophthalmology. Journal Canadien d’ophtalmologie. https://doi.org/10.1016/j.jcjo.2024.02.010

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Experimental vaccine found effective against both ocular trachoma and urogenital chlamydia in Phase 1 trial: Lancet

Initial results from a recent Phase 1 clinical trial indicate that the experimental vaccine CTH522 could be a crucial tool against both ocular trachoma and urogenital chlamydia. The key findings were published in The Lancet Infectious Diseases

The CHLM-02 trial was conducted at the National Institute for Health Research Imperial Clinical Research Facility in London, UK. It involved healthy male and female participants from 18 to 45 years, all of whom were free from any pre-existing genital infections caused by C. trachomatis. This double-blind, randomized, placebo-controlled trial assessed the safety and immunogenicity of various dosing regimens of the vaccine candidate CTH522 which is a recombinant protein based on the major outer membrane molecule of bacterium.

The participants were divided into six groups where five groups received the vaccine in different dosing formats and combinations, and one group receiving a placebo. The vaccine was administered intramuscularly, intradermally and topically into the eye in prime-boost regimens by utilizing two different liposomal adjuvants, the CAF01 and CAF09b.

The results from the trial from February 2020 to February 2022 were highly encouraging. A total of 65 participants were enrolled where 60 participants completed the trial. The study reported no serious adverse events and the majority of side effects were mild to moderate. Also, a 100% seroconversion rate was observed by day 42 in all active vaccine groups that indicates a significant immune response.

The different administration routes seemed to improve vaccine efficacy against specific types of infections. The intradermal administration of CTH522 led to high titers of neutralizing antibodies against the serovars linked with trachoma and genital infections. The topical ocular administration significantly elevated ocular IgA levels which suggested potential effectiveness against ocular trachoma.

The primary outcome of the trial was to evaluate safety while the secondary outcome focused on humoral immunogenicity, specifically the percentage of the participants who achieved a significant increase in anti-CTH522 IgG antibody levels. The findings suggest that CTH522 when adjuvanted with CAF01, induced robust serum IgG binding titers. Also, participants developed strong cell-mediated immune responses in groups who received the vaccine with the CAF09b adjuvant. Further research through the Phase 2 clinical trials would test effectiveness of CTH522 in larger populations. If successful, this vaccine candidate could become a critical resource in controlling and potentially eradicating infections caused by C. trachomatis.

Reference:

Pollock, K. M., Borges, Á. H., Cheeseman, H. M., Rosenkrands, I., Schmidt, K. L., Søndergaard, R. E., Day, S., Evans, A., McFarlane, L. R., Joypooranachandran, J., Amini, F., Skallerup, P., Dohn, R. B., Jensen, C. G., Olsen, A. W., Bang, P., Cole, T., Schronce, J., Lemm, N.-M., … Follmann, F. (2024). An investigation of trachoma vaccine regimens by the chlamydia vaccine CTH522 administered with cationic liposomes in healthy adults (CHLM-02): a phase 1, double-blind trial. In The Lancet Infectious Diseases. Elsevier BV. https://doi.org/10.1016/s1473-3099(24)00147-6

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Gauhati Medical College PG Gynaecology medico expelled for 1 year over allegations of slapping pregnant woman

Guwahati: A third-year PG medico at the Department of Obstetrics and Gynaecology of Gauhati Medical College Hospital (GMCH) has been expelled by the college administration for a year after allegations were levelled against him of hitting a pregnant woman in the hospital.

The incident reportedly took place in the labour room of the hospital. Sources informed TOI that the medico got angry when the woman reportedly spit on and shouted at him. In reply, the doctor slapped her in the face, the source said, as quoted by TOI.

It was alleged that the doctor had assaulted the patient in the labour room leading to bruises on the patient’s face. Images of the bruised face of the patient were shared over social media, leading the authorities to take immediate action on the matter.

Subsequently, the GMCH authorities constituted a four-member inquiry committee to probe the allegations. According to an inquiry order, the committee was asked to submit a report on the allegation of physical assault by PGT of O&G to one admitted case in the O&G department of GMCH.

This committee was chaired by Dr BP Das, Prof and HOD of the O&G Department and comprised of Dr Kanakeswar Bhuyan, Prof and HOD of the Surgery Department as a member, Dr Pankaj Adhikari, Prof and HOD of the Dermatology Department as the Member Secretary and Dr Pradip Kr Das, Additional Superintendent of GMCH as a Member. The committee was ordered to investigate the matter and submit the report within 24 hours, reports Sentinel Assam.

Speaking to TOI, GMCH medical superintendent Abhijit Sarma said “Dr ** is a third-year PG student and has been expelled from the course for a year. After one year, we will decide whether he should be given a further chance to study.”

Also read- Dereliction Of Duty: Medical Officer Faces Suspension, Another Under Radar Of JnK Health Dept

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Dr.Reddy’s Labs gets CDSCO Panel Nod To Manufacture, Market anti-cancer drug Lenalidomide 20mg additional strength

New Delhi: The drug major Dr Reddy’s Labs has got a go-ahead from the Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) to manufacture and market the anti-cancer drug Lenalidomide capsules 20mg (additional strength) with Phase-III clinical trial (CT) waiver.

This came after Dr.Reddy’s Labs presented the proposal for manufacturing and marketing permission for Lenalidomide capsules 20mg (additional strength) along with justification for the waiver of Phase-III CT with Bioequivalence study report of Lenalidomide capsules 25mg before the committee.

The firm has informed that the proposed formulation strength 5mg 10 mg, 15mg, and 25 mg of Lenalidomide Capsules 20mg are already approved by CDSCO since 2007 in the country. The proposed strength 20 mg of Lenalidomide capsules are only for dose titration purposes only.

Lenalidomide is a thalidomide derivative used to treat multiple myeloma and anemia in low to intermediate-risk myelodysplastic syndrome. Lenalidomide is an immunomodulatory drug with potent antineoplastic, anti-angiogenic, and anti-inflammatory properties.

Lenalidomide is a drug with multiple mechanisms of action. Lenalidomide exerts immunomodulating effects by altering cytokine production, regulating T-cell co-stimulation, and enhancing NK cell-mediated cytotoxicity.

At the recent SEC meeting for Oncology held on 3rd and 4th April 2024, the expert panel reviewed the proposal presented by the drug major Dr Reddy’s Labs to manufacture and market Lenalidomide capsules 20mg (additional strength) along with justification for the waiver of Phase-III CT with Bioequivalence study report of Lenalidomide capsules 25mg before the committee.

After detailed deliberation, the committee recommended the grant of permission to manufacture and market Lenalidomide capsules 20mg (additional strength) with a Phase-III clinical trial waiver.

Also Read: Bharath Biotech Gets CDSCO Panel Nod To Manufacture Cholera Vaccine, Inactivated, Oral for 1 year age and above

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Mac-Chem Products Boisar facility Successfully Renews EU GMP Certification

Mumbai: Mac-Chem Products (India) Pvt. Ltd. (Mac-Chem) announced today the successful renewal of its European Union Goods Manufacturing Practices) (EU-GMP certification for its manufacturing facility in Boisar. The approval marks a significant milestone for Mac-Chem in its journey of global leadership. The audit was conducted in October 2023 by Swissmedic Swiss Agency for Therapeutic Products. 

Speaking on the development, Mr. Manish Jain, Director at Mac-Chem said, “We are delighted with the successful renewal of our EU-GMP certification. The achievement affirms our commitment to the highest standards of quality and compliance aligning with the European regulations.
The timely approval further reaffirms our commitment for delivering high-quality pharma products that positively impact patient care globally.”
The EU-GMP certification underlines the Boisar facility’s capabilities to ensure consistent and controlled production in accordance with EU quality standards. The facility produces a wide range of APIs, with a special focus on oncology and other niche specialty segments.

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